Recurrent 16p11.2 microdeletions in autism.

Kumar, Ravinesh A

Recurrent 16p11.2 microdeletions in autism. [electronic resource] - Human molecular genetics Feb 2008 - 628-38 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

1460-2083

10.1093/hmg/ddm376 doi


Autistic Disorder--genetics
Base Sequence
Case-Control Studies
Child
Chromosome Breakage
Chromosome Deletion
Chromosomes, Artificial, Bacterial--genetics
Chromosomes, Human, Pair 16--genetics
DNA Primers--genetics
Female
Gene Frequency
Genetic Predisposition to Disease
Humans
In Situ Hybridization, Fluorescence
Male
Microsatellite Repeats
Pedigree
Phenotype
Polymerase Chain Reaction