(Q36927121)

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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

scientific article published on 13 July 2006

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Europe PubMed Central

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27 December 2019

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders (English)

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27 December 2019

autism spectrum disorder

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27 December 2019

Damien Sanlaville

2

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27 December 2019

Valérie Cormier-Daire

5

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27 December 2019

Stanislas Lyonnet

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27 December 2019

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27 December 2019

Laurence Colleaux

15

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27 December 2019

16

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27 December 2019

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M-L Jacquemont

1

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27 December 2019

O Raoul

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27 December 2019

M Le Merrer

8

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27 December 2019

D Heron

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27 December 2019

M-C de Blois

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27 December 2019

M Prieur

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27 December 2019

M Vekemans

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27 December 2019

N P Carter

13

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27 December 2019

A Munnich

14

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27 December 2019

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13 July 2006

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27 December 2019

Journal of Medical Genetics

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27 December 2019

43

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27 December 2019

11

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27 December 2019

843-849

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27 December 2019

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

1 reference

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29 September 2017

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

1 reference

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Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.

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Molecular cytogenetics of mouse models of breast cancer

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Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

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29 September 2017

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

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29 September 2017

Detection of large-scale variation in the human genome

1 reference

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29 September 2017

Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum

1 reference

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29 September 2017

Large-scale copy number polymorphism in the human genome

1 reference

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29 September 2017

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563185

29 September 2017

Autism and pervasive developmental disorders

1 reference

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29 September 2017

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities

1 reference

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29 September 2017

Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

1 reference

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29 September 2017

Epidemiological surveys of autism and other pervasive developmental disorders: an update

1 reference

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29 September 2017

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

1 reference

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29 September 2017

DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

1 reference

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29 September 2017

The prevalence of autism

1 reference

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29 September 2017

High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization

1 reference

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Fully automatic quantification of microarray image data

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29 September 2017

Genetics of austim: complex aetiology for a heterogeneous disorder

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29 September 2017

45,X/46,XY mosaicism: report of 27 cases

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29 September 2017

Deletion of chromosome 2q37 and autism: a distinct subtype?

1 reference

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29 September 2017

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

1 reference

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29 September 2017

Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey

1 reference

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29 September 2017

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

1 reference

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29 September 2017

Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances

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29 September 2017

A case-control family history study of autism

1 reference

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29 September 2017

Infantile autism: a genetic study of 21 twin pairs

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Xp deletions associated with autism in three females

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18q- chromosomal abnormality in a phenotypically normal 2 1/2-year-old male with autism

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4 September 2018

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH

1 reference

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Fluorescence genotyping for screening cryptic telomeric rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/16840569

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A tiling resolution DNA microarray with complete coverage of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16840569

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.2006.043166

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16840569 AND SRC:MED&resulttype=core&format=json

27 December 2019

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16840569 AND SRC:MED&resulttype=core&format=json

27 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

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27 December 2019

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