TY  - GEN
AU  - Kariminejad,Roxana
AU  - Lind-Thomsen,Allan
AU  - Tümer,Zeynep
AU  - Erdogan,Fikret
AU  - Ropers,Hans H
AU  - Tommerup,Niels
AU  - Ullmann,Reinhard
AU  - Møller,Rikke S
TI  - High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations
SN  - 1098-1004
PY  - 2012///0327
KW  - Agenesis of Corpus Callosum
KW  - diagnostic imaging
KW  - Brain
KW  - Child
KW  - Child, Preschool
KW  - Cohort Studies
KW  - Comparative Genomic Hybridization
KW  - DNA Copy Number Variations
KW  - genetics
KW  - Epilepsy
KW  - Female
KW  - Gene Dosage
KW  - Gene Frequency
KW  - Humans
KW  - Intellectual Disability
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Nervous System Malformations
KW  - Phenotype
KW  - Proteins
KW  - Radiography
KW  - Tomography Scanners, X-Ray Computed
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/humu.21585
ER  -