Advanced technologies for the molecular diagnosis of fragile X syndrome (Q28087781)

language of work or name

1 reference

2015

1 reference

Expert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcare

published in

1 reference

volume

15

1 reference

issue

11

1 reference

page(s)

1465-73

1 reference

Fragile X-associated tremor/ataxia syndrome

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Fragile X spectrum disorders

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

The multiple molecular facets of fragile X-associated tremor/ataxia syndrome

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Use of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI)

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Sequencing the unsequenceable: expanded CGG-repeat alleles of the fragile X gene

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Bisulfite genomic sequencing: systematic investigation of critical experimental parameters

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

High sensitivity mapping of methylated cytosines

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Trinucleotide repeats that expand in human disease form hairpin structures in vitro

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Trajectory and Predictors of Depression and Anxiety Disorders in Mothers With the FMR1 Premutation

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Validation of a Commercially Available Screening Tool for the Rapid Identification of CGG Trinucleotide Repeat Expansions in FMR1.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Delineation of the working memory profile in female FMR1 premutation carriers: the effect of cognitive load on ocular motor responses.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Clinical and molecular implications of mosaicism in FMR1 full mutations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

The cognitive neuropsychological phenotype of carriers of the FMR1 premutation.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Associated features in females with an FMR1 premutation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Visual motion processing deficits in infants with the fragile X premutation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Translating molecular advances in fragile X syndrome into therapy: a review

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Newborn screening for fragile X syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Offering fragile X syndrome carrier screening: a prospective mixed-methods observational study comparing carrier screening of pregnant and non-pregnant women in the general population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

FMR1 CGG expansions: prevalence and sex ratios

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

The translation of translational control by FMRP: therapeutic targets for FXS.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Development of a fragile X syndrome (FXS) knowledge scale: towards a modified multidimensional measure of informed choice for FXS population carrier screening

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Fragile X-associated tremor/ataxia syndrome (FXTAS) in grey zone carriers

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Fragile X-associated tremor ataxia syndrome in FMR1 gray zone allele carriers

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

High-resolution methylation polymerase chain reaction for fragile X analysis: Evidence for novel FMR1 methylation patterns undetected in Southern blot analyses

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

A simple, high-throughput assay for Fragile X expanded alleles using triple repeat primed PCR and capillary electrophoresis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Principles and challenges of genomewide DNA methylation analysis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Mutation spectra in fragile X syndrome induced by deletions of CGG*CCG repeats

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Methylation-specific multiplex ligation-dependent probe amplification enables a rapid and reliable distinction between male FMR1 premutation and full-mutation alleles

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Fragile X syndrome: diagnostic and carrier testing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Screening for fragile X syndrome: a literature review and modelling study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Standardization of PCR amplification for fragile X trinucleotide repeat measurements

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Fragile X syndrome: a model of gene-brain-behavior relationships

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Methylation analysis of the fragile X syndrome by PCR.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Automated Detection of Trinucleotide Repeats in Fragile X Syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Fragile-X syndrome: unique genetics of the heritable unstable element

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Autism profiles of males with fragile X syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

A clinicopathological study of autism

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Excess thymidine induces folate sensitive fragile sites

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Absence of expression of the FMR-1 gene in fragile X syndrome

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

DNA methylation represses FMR-1 transcription in fragile X syndrome

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders

2 June 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

SnapShot: FMRP mRNA targets and diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Autism spectrum phenotype in males and females with fragile X full mutation and premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Mosaicism in fragile X affected males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Prenatal diagnosis and carrier screening for fragile X by PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Improved fluorescent PCR-based assay for sizing CGG repeats at the FRAXA locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

A simple and rapid analysis of triplet repeat diseases by expand long PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: implications for fragile X syndrome carrier and newborn screening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Development of a novel, accurate, automated, rapid, high-throughput technique suitable for population-based carrier screening for Fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Evaluation of the human fragile X mental retardation 1 polymerase chain reaction reagents to amplify the FMR1 gene: testing in a clinical diagnostic laboratory

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Comparison between the polymerase chain reaction-based screening and the Southern blot methods for identification of fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

PCR approach for detection of Fragile X syndrome and Huntington disease based on modified DNA: limits and utility

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Robust fragile X (CGG)n genotype classification using a methylation specific triple PCR assay

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

A homogeneous assay for analysis of FMR1 promoter methylation in patients with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Cost-effectiveness analysis of prenatal population-based fragile X carrier screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and Children

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

Women's attitudes toward testing for fragile X carrier status: a qualitative analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1586/14737159.2015.1101348

A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4955806

Fragile X syndrome: is now the time for population screening?

27 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/26489042

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

"It's something I need to consider": decisions about carrier screening for fragile X syndrome in a population of non-pregnant women

1 reference

https://pubmed.ncbi.nlm.nih.gov/26489042

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Newborn screening: evolving challenges in an era of rapid discovery

1 reference

https://pubmed.ncbi.nlm.nih.gov/26489042

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1586/14737159.2015.1101348

1 reference

1 reference

1 reference

PubMed publication ID

26489042

1 reference