Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics (Q30391597)

16 August 2017

Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics (English)

1 reference

16 August 2017

whole genome sequencing

1 reference

inferred from title

author

Hanne Meijers-Heijboer

10

Hanne Meijers-Heijboer

0 references

Anne Cambon-Thomsen

8

Anne Cambon-Thomsen

0 references

Bartha Knoppers

9

Bartha M Knoppers

1 reference

16 August 2017

3

Pascal Borry

0 references

Heidi Carmen Howard

7

Heidi C Howard

1 reference

16 August 2017

2

Martina C Cornel

1 reference

16 August 2017

13

Wybo Dondorp

1 reference

16 August 2017

12

Lisbeth Tranebjaerg

1 reference

16 August 2017

1

Carla G van El

1 reference

16 August 2017

Ros J Hastings

4

1 reference

16 August 2017

Florence Fellmann

5

1 reference

16 August 2017

Shirley V Hodgson

6

1 reference

16 August 2017

Hans Scheffer

11

1 reference

16 August 2017

Guido M W R de Wert

14

1 reference

16 August 2017

ESHG Public and Professional Policy Committee

15

1 reference

16 August 2017

1 June 2013

1 reference

European Journal of Human Genetics

16 August 2017

1 reference

16 August 2017

21 Suppl 1

1 reference

16 August 2017

S1-5

1 reference

Diagnostic interpretation of array data using public databases and internet sources

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

De novo mutations in human genetic disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Developing a policy for paediatric biobanks: principles for good practice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Noninvasive whole-genome sequencing of a human fetus.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Incidental medical information in whole-exome sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

The predictive capacity of personal genome sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

The ethical hazards and programmatic challenges of genomic newborn screening

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Preconceptional genetic carrier testing and the commercial offer directly-to-consumers

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Genetic testing and common disorders in a public health framework

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Carrier testing for severe childhood recessive diseases by next-generation sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Disclosure of individual genetic data to research participants: the debate reconsidered

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

A map of human genome variation from population-scale sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Clinical assessment incorporating a personal genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Personal genomes in progress: from the human genome project to the personal genome project

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Non-invasive prenatal testing: ethical issues explored

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Exome sequencing identifies the cause of a mendelian disorder

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Genetic testing in asymptomatic minors: Recommendations of the European Society of Human Genetics

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testing.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

The complete genome of an individual by massively parallel DNA sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

GENE SEQUENCING: The Race for the $1000 Genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues.

20 June 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Preimplantation genetic screening: a systematic review and meta-analysis of RCTs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Next generation sequencing allows deeper analysis and understanding of genomes and transcriptomes including aspects to fertility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Comprehensive pre-implantation genetic screening: ethical reflection urgently needed

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Reproductive technologies and the risk of birth defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Increased risk of blastogenesis birth defects, arising in the first 4 weeks of pregnancy, after assisted reproductive technologies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Imprinting disorders and assisted reproductive technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The ESHRE PGD Consortium: 10 years of data collection

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Cross border reproductive care in six European countries

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The long-term fiscal impact of funding cuts to Danish public fertility clinics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Stem cells and fertility: what does the future hold?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

When and how should new technology be introduced into the IVF laboratory?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The clinical benefit and safety of current and future assisted reproductive technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Does the European Union Tissues and Cells Directive improve quality in the in vitro fertilization laboratory? A case study in a tertiary referral center

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

CBRC and psychosocial counselling: assessing needs and developing an ethical framework for practice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

ESHRE task force on ethics and law 15: cross-border reproductive care

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

ESHRE's good practice guide for cross-border reproductive care for centers and practitioners

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Comparison of concomitant outcome achieved with fresh and cryopreserved donor oocytes vitrified by the Cryotop method

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Implications of oocyte cryostorage for the practice of oocyte donation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Guidelines for the appropriate use of genetic tests in infertile couples.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

FOXL2 mutations and genomic rearrangements in BPES.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Five mutations of mitochondrial DNA polymerase-gamma (POLG) are not a prevalent etiology for spontaneous 46,XX primary ovarian insufficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Primary ovarian insufficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genes involved in human premature ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Molecular pathogenesis of Kallmann's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Androgen insensitivity syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genetic aspects of female reproduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genetics of recurrent miscarriage: challenges, current knowledge, future directions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Recurrent miscarriage and thrombophilia: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

A proposal for reproductive counselling in carriers of Robertsonian translocations: 10 years of experience with preimplantation genetic diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Preimplantation genetic diagnosis in female and male carriers of reciprocal translocations: clinical outcome until delivery of 312 cycles

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Increased frequency of the DI genotype of the angiotensin-I converting enzyme and association of the II genotype with insulin resistance in polycystic ovary syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Insights into Assessing the Genetics of Endometriosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Deciphering genetic disease in the genomic era: the model of GnRH deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

World Health Organization reference values for human semen characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Male infertility: pathogenesis and clinical diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Update on surgical sperm recovery – The European view

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genetic evaluation of the azoospermic or severely oligozoospermic male

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The genetic origin of Klinefelter syndrome and its effect on spermatogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Spermatogonial stem cell preservation in boys with Klinefelter syndrome: to bank or not to bank, that's the question

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Balanced complex chromosome rearrangements: reproductive aspects. A review.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Cystic fibrosis transmembrane conductance regulator is vital to sperm fertilizing capacity and male fertility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Clinical consequences of microdeletions of the Y chromosome: the extended Münster experience

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Clinical Review#: State of the art for genetic testing of infertile men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genetic dissection of the AZF regions of the human Y chromosome: thriller or filler for male (in)fertility?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Clinical data and parenthood of 63 infertile and Y-microdeleted men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Y chromosome gr/gr deletions are a risk factor for low semen quality

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Clinical manifestations of impaired GnRH neuron development and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Oligogenic basis of isolated gonadotropin-releasing hormone deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Male infertility and androgen receptor gene mutations: clinical features and identification of seven novel mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Gene polymorphisms and male infertility--a meta-analysis and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genome-wide association study identifies candidate genes for male fertility traits in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Molecular cytogenetic and genetic aspects of globozoospermia: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Sperm macrocephaly syndrome in a patient without AURKC mutations and with a history of recurrent miscarriage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Mitochondria-related male infertility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The effect of obesity on sperm disorders and male infertility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Influence of endocrine disruptors on human male fertility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Challenging cell phone impact on reproduction: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

A review of genome-wide approaches to study the genetic basis for spermatogenic defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

International normative perspectives on the return of individual research results and incidental findings in genomic biobanks

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Proteomic insights into the maturation and capacitation of mammalian spermatozoa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The genetics of male fertility--from basic science to clinical evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

What is ideal genetic counselling? A survey of current international guidelines

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Neonatal follow-up of 995 consecutively born children after embryo biopsy for PGD

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Coming soon to your clinic: patient-friendly ART.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Robert Edwards: the path to IVF.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genetic education and the challenge of genomic medicine: development of core competences to support preparation of health professionals in Europe

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Using a community of practice to develop standards of practice and education for genetic counsellors in Europe

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Assisted reproductive technology, epigenetics, and long-term health: a developmental time bomb still ticking

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Conceptualizing couples' decision making in PGD: emerging cognitive, emotional, and moral dimensions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The decision-making process of genetically at-risk couples considering preimplantation genetic diagnosis: initial findings from a grounded theory study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

New perspectives on embryo biopsy: not how, but when and why?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

ESHRE PGD Consortium data collection XI: cycles from January to December 2008 with pregnancy follow-up to October 2009.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Birth of a healthy infant following trophectoderm biopsy from blastocysts for PGD of beta-thalassaemia major.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Pregnancies and live births after trophectoderm biopsy and preimplantation genetic testing of human blastocysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Current aspects of blastocyst cryopreservation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Preimplantation genetic diagnosis: State of the ART 2011

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The use of arrays in preimplantation genetic diagnosis and screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The causes of misdiagnosis and adverse outcomes in PGD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Preimplantation genetic haplotyping: 127 diagnostic cycles demonstrating a robust, efficient alternative to direct mutation testing on single cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Aneuploidy in the Human Blastocyst

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Validation of microarray comparative genomic hybridization for comprehensive chromosome analysis of embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Gamete donation and anonymity: the ethical and legal debate

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

What next for preimplantation genetic screening? A polar body approach!

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Does additional hybridization also improve preimplantation genetic screening results?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium Steering Committee

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Polar body array CGH for prediction of the status of the corresponding oocyte. Part I: clinical results

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Comprehensive chromosome screening is highly predictive of the reproductive potential of human embryos: a prospective, blinded, nonselection study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

ESHRE PGD consortium best practice guidelines for organization of a PGD centre for PGD/preimplantation genetic screening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Accreditation of the PGD laboratory

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

A high degree of aneuploidy in frozen-thawed human preimplantation embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Chromosomal mosaicism in human preimplantation embryos: a systematic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Chromosome instability is common in human cleavage-stage embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

New array approaches to explore single cells genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Detection of unbalanced chromosome segregations in preimplantation genetic diagnosis of translocations by short comparative genomic hibridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Application of next generation sequencing in mammalian embryogenomics: lessons learned from endogenous betaretroviruses of sheep

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Tumour evolution inferred by single-cell sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The 'thousand-dollar genome': an ethical exploration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Ethical issues in infertility treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Benchmark for evaluating the quality of DNA sequencing: proposal from an international external quality assessment scheme

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

An international external quality assessment for molecular diagnosis of hereditary recurrent fevers: a 3-year scheme demonstrates the need for improvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Quality assurance practices in Europe: a survey of molecular genetic testing laboratories

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

An Internet-based external quality assessment in cytogenetics that audits a laboratory's analytical and interpretative performance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Variability in the use of CE-marked assays for in vitro diagnostics of CFTR gene mutations in European genetic testing laboratories

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

A standardized framework for the validation and verification of clinical molecular genetic tests

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Provision and quality assurance of preimplantation genetic diagnosis in Europe

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Letting the genome out of the bottle--will we get our wish?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

DTC Genetic Services: A Look Across the Pond

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Users' motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The changing privacy landscape in the era of big data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Three-month follow-up of Western and non-Western participants in a study on preconceptional ancestry-based carrier couple screening for cystic fibrosis and hemoglobinopathies in the Netherlands

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Benchmarks for cystic fibrosis carrier screening: a European consensus document

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Research 2.0: social networking and direct-to-consumer (DTC) genomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Linking genome to epigenome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Transgenerational Epigenetic Inheritance: Prevalence, Mechanisms, and Implications for the Study of Heredity and Evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Assisted reproduction treatment and epigenetic inheritance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Epigenetic reprogramming in plant and animal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Effect of in vitro culture of human embryos on birthweight of newborns

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Epigenetics, genomic imprinting and assisted reproductive technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Imprinting diseases and IVF: Danish National IVF cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Teratogen update: carcinogenesis and teratogenesis associated with exposure to diethylstilbestrol (DES) in utero

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Assisted reproductive technology and major structural birth defects in the United States

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Maternal and child outcome after in vitro fertilization--a review of 25 years of population-based data from Sweden

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Expanding the boundaries of embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Diseases in a dish: modeling human genetic disorders using induced pluripotent cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

iPSC technology to study human aging and aging-related disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Recurrent chromosomal abnormalities in human embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

A poor imitation of a natural process: a call to reconsider the iPSC engineering technique

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Improving health systems and enhancing reproductive health: linkages and lessons for action

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Negative lifestyle is associated with a significant reduction in fecundity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Swedish high school students' knowledge and attitudes regarding fertility and family building

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Demographic and medical consequences of the postponement of parenthood

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Adoption in the age of reproductive technology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Economics of assisted reproduction: access to fertility treatments and valuing live births in economic terms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

21 January 2018

A right to reproduce?

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Infertility, assisted reproduction and rights.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

In vitro fertilisation policy in Israel and women's perspectives: the more the better?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Public financing of IVF: a review of policy rationales.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Shared lesbian motherhood: a challenge of established concepts and frameworks

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Measuring the welfare of the child: in search of the appropriate evaluation principle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Evaluation of exclusion prenatal and exclusion preimplantation genetic diagnosis for Huntington's disease in the Netherlands.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

ESHRE Task Force on ethics and Law 20: sex selection for non-medical reasons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Preimplantation genetic diagnosis: the ethics of intermediate cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Serious genetic disorders: can or should they be defined?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Dealing with uncertainties: ethics of prenatal diagnosis and preimplantation genetic diagnosis to prevent mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Preventing transmission of maternally inherited mitochondrial DNA diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Reproductive decision-making in the context of mitochondrial DNA disorders: views and experiences of professionals

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Intrafamilial medically assisted reproduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Ethics of modifying the mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The ART of social networking: how SART member clinics are connecting with patients online

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

What is the impact of the Internet on decision-making in pregnancy? A global study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Cascade testing in familial hypercholesterolaemia: how should family members be contacted?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Preconception care and genetic risk: ethical issues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genetic counselling for personalised medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Recommendations for gamete and embryo donation: a committee opinion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genetic screening of sperm and oocyte donors: ethical and policy implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Implications of Hypertrophic Cardiomyopathy Transmitted by Sperm Donation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genetic testing of sperm donors: survey of current practices

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Dynamics and ethics of comprehensive preimplantation genetic testing: a review of the challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

THE MORAL OBLIGATION TO CREATE CHILDREN WITH THE BEST CHANCE OF THE BEST LIFE

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Get ready for the flood of fetal gene screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The consequences of S.H. and Others v. Austria for legislation on gamete donation in Europe: an ethical analysis of the European Court of Human Rights judgments

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Idiopathic recurrent miscarriage is caused mostly by aneuploid embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Increased rate of aneuploid embryos in young women with previous aneuploid conceptions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Genomic anonymity: have we already lost it?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Direct-to-consumer genome scanning services. Also for children?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The need for interaction between assisted reproduction technology and genetics: recommendations of the European Societies of Human Genetics and Human Reproduction and Embryology*

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The need for interaction between assisted reproduction technology and genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxias

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

Is cascade testing a sensible method of population screening?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

The use of arrays to detect copy-number variations in clinical practice

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Whole-genome sequencing and the physician

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

A de novo paradigm for mental retardation

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Screening using whole-body magnetic resonance imaging scanning: who wants an incidentaloma?

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3660957

Communication of biobanks' research results: what do (potential) participants want?

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23819146

12 December 2020

inferred from PubMed ID database lookup

Between hype and hope: whole-genome sequencing in clinical medicine

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23819146

12 December 2020

inferred from PubMed ID database lookup

Assisted reproduction and genetics

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Europe and direct-to-consumer genetic tests

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Genomic medicine: challenges and opportunities for physicians

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Does assisted reproductive treatment increase the risk of birth defects in the offspring?

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

ESHRE Task Force on Ethics and Law 14: equity of access to assisted reproductive technology

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Cross-border reproductive services: FIGO Committee for the Ethical Aspects of Human Reproduction and Women's Health

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

The pluralism problem in cross-border reproductive care

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Combination of enzyme analysis, allele-specific PCR and sequencing to detect mutations in the GALT gene

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

The prevalence of chromosomal abnormalities in subgroups of infertile men

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

TESE-ICSI in patients with non-mosaic Klinefelter syndrome: a comparative study

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Clinical experience with azoospermia: aetiology and chances for spermatozoa detection upon biopsy

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Significance of CFTR gene mutations in patients with congenital aplasia of vas deferens with special regard to renal aplasia

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

ESHRE Task Force on Ethics and Law 13: the welfare of the child in medically assisted reproduction

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Women's experience of pre-implantation genetic diagnosis: a qualitative study

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

ESHRE PGD Consortium/Embryology Special Interest Group--best practice guidelines for polar body and embryo biopsy for preimplantation genetic diagnosis/screening (PGD/PGS)

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

ESHRE PGD consortium best practice guidelines for amplification-based PGD

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

ESHRE PGD consortium best practice guidelines for fluorescence in situ hybridization-based PGD

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

First births after preimplantation genetic diagnosis of structural chromosome abnormalities using comparative genomic hybridization and microarray analysis

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Single nucleotide polymorphism microarray-based concurrent screening of 24-chromosome aneuploidy and unbalanced translocations in preimplantation human embryos

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Karyomapping: a universal method for genome wide analysis of genetic disease based on mapping crossovers between parental haplotypes

1 reference

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7 January 2021

Reproductive decisions after fetal genetic counselling

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation, (FISH)

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Preimplantation genetic screening reveals a high incidence of aneuploidy and mosaicism in embryos from young women undergoing IVF

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

High incidence of complex chromosome abnormality in cleavage embryos from patients with repeated implantation failure

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https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridization

1 reference

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7 January 2021

Innovative reproductive technologies: risks and responsibilities

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Genome test slammed for assessing ‘racial purity’

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Epigenetic change in IGF2R is associated with fetal overgrowth after sheep embryo culture

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Assisted reproductive therapies and imprinting disorders--a preliminary British survey

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Infertility, assisted reproduction technologies and imprinting disturbances: a Dutch study

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Imprinting disorders and assisted reproductive technology.

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

On the ability of birth defects monitoring to detect new teratogens

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Human embryonic stem cells commonly display large mitochondrial DNA deletions

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Germany allows restricted access to preimplantation genetic testing

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Preimplantation genetic diagnosis

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

[Preimplantation genetic diagnosis in order to choose a saviour sibling]

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Preimplantation genetic diagnosis comes of age

1 reference

https://api.crossref.org/works/10.1038/EJHG.2013.219

7 January 2021

Identifiers

DOI

10.1038/EJHG.2013.219

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

23819146

1 reference