TY  - GEN
AU  - Nava,Caroline
AU  - Keren,Boris
AU  - Mignot,Cyril
AU  - Rastetter,Agnès
AU  - Chantot-Bastaraud,Sandra
AU  - Faudet,Anne
AU  - Fonteneau,Eric
AU  - Amiet,Claire
AU  - Laurent,Claudine
AU  - Jacquette,Aurélia
AU  - Whalen,Sandra
AU  - Afenjar,Alexandra
AU  - Périsse,Didier
AU  - Doummar,Diane
AU  - Dorison,Nathalie
AU  - Leboyer,Marion
AU  - Siffroi,Jean-Pierre
AU  - Cohen,David
AU  - Brice,Alexis
AU  - Héron,Delphine
AU  - Depienne,Christel
TI  - Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders
SN  - 1476-5438
PY  - 2015///0212
KW  - Adolescent
KW  - Child
KW  - Child Development Disorders, Pervasive
KW  - etiology
KW  - Child, Preschool
KW  - Chromosomes, Human, Pair 15
KW  - genetics
KW  - Chromosomes, Human, Pair 5
KW  - Comparative Genomic Hybridization
KW  - Cri-du-Chat Syndrome
KW  - DNA Copy Number Variations
KW  - DNA Methylation
KW  - Female
KW  - Genetic Association Studies
KW  - Genotype
KW  - Humans
KW  - Infant
KW  - Male
KW  - Oligonucleotide Array Sequence Analysis
KW  - methods
KW  - Polymorphism, Single Nucleotide
KW  - Trisomy
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/ejhg.2013.88
ER  -