TY  - GEN
AU  - Mignon-Ravix,Cécile
AU  - Cacciagli,Pierre
AU  - Choucair,Nancy
AU  - Popovici,Cornel
AU  - Missirian,Chantal
AU  - Milh,Mathieu
AU  - Mégarbané,André
AU  - Busa,Tiffany
AU  - Julia,Sophie
AU  - Girard,Nadine
AU  - Badens,Catherine
AU  - Sigaudy,Sabine
AU  - Philip,Nicole
AU  - Villard,Laurent
TI  - Intragenic rearrangements in X-linked intellectual deficiency: results of a-CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes
SN  - 1552-4833
PY  - 2015///0331
KW  - Child, Preschool
KW  - Chromosome Mapping
KW  - Chromosomes, Human, X
KW  - Comparative Genomic Hybridization
KW  - DNA Copy Number Variations
KW  - Gene Deletion
KW  - Genes, X-Linked
KW  - Genetic Loci
KW  - Genome-Wide Association Study
KW  - Humans
KW  - Intellectual Disability
KW  - diagnosis
KW  - Male
KW  - Microfilament Proteins
KW  - genetics
KW  - TRPC Cation Channels
KW  - Translocation, Genetic
KW  - X Chromosome Inactivation
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.36602
ER  -