High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations.
Kariminejad, Roxana
High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations. [electronic resource] - Human mutation Dec 2011 - 1427-35 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1098-1004
10.1002/humu.21585 doi
Agenesis of Corpus Callosum--diagnostic imaging
Brain--diagnostic imaging
Child
Child, Preschool
Cohort Studies
Comparative Genomic Hybridization
DNA Copy Number Variations--genetics
Epilepsy--diagnostic imaging
Female
Gene Dosage--genetics
Gene Frequency
Humans
Intellectual Disability--diagnostic imaging
Magnetic Resonance Imaging
Male
Nervous System Malformations--diagnostic imaging
Phenotype
Proteins--genetics
Radiography
Tomography Scanners, X-Ray Computed
High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations. [electronic resource] - Human mutation Dec 2011 - 1427-35 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1098-1004
10.1002/humu.21585 doi
Agenesis of Corpus Callosum--diagnostic imaging
Brain--diagnostic imaging
Child
Child, Preschool
Cohort Studies
Comparative Genomic Hybridization
DNA Copy Number Variations--genetics
Epilepsy--diagnostic imaging
Female
Gene Dosage--genetics
Gene Frequency
Humans
Intellectual Disability--diagnostic imaging
Magnetic Resonance Imaging
Male
Nervous System Malformations--diagnostic imaging
Phenotype
Proteins--genetics
Radiography
Tomography Scanners, X-Ray Computed