Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders (Q36927121)

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scientific article published on 13 July 2006

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English	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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scholarly article

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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

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27 December 2019

Valérie Cormier-Daire

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27 December 2019

Stanislas Lyonnet

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27 December 2019

Laurence Colleaux

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27 December 2019

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M-L Jacquemont

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27 December 2019

O Raoul

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27 December 2019

M Le Merrer

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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

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27 December 2019

A Munnich

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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

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27 December 2019

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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

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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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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

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29 September 2017

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

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29 September 2017

Large-scale copy number polymorphism in the human genome

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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

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29 September 2017

Autism and pervasive developmental disorders

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29 September 2017

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

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29 September 2017

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

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29 September 2017

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

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29 September 2017

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

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

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

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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?

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

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29 September 2017

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

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29 September 2017

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

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

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A case-control family history study of autism

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Autism as a strongly genetic disorder: evidence from a British twin study

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A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

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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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BAC array CGH reveals genomic aberrations in idiopathic mental retardation.

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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

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Fluorescence genotyping for screening cryptic telomeric rearrangements

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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

12 December 2020

based on heuristic

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Identifiers

10.1136/JMG.2006.043166

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27 December 2019

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27 December 2019

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27 December 2019

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