TY  - GEN
AU  - Kumar,Ravinesh A
AU  - KaraMohamed,Samer
AU  - Sudi,Jyotsna
AU  - Conrad,Donald F
AU  - Brune,Camille
AU  - Badner,Judith A
AU  - Gilliam,T Conrad
AU  - Nowak,Norma J
AU  - Cook,Edwin H
AU  - Dobyns,William B
AU  - Christian,Susan L
TI  - Recurrent 16p11.2 microdeletions in autism
SN  - 1460-2083
PY  - 2008///0312
KW  - Autistic Disorder
KW  - genetics
KW  - Base Sequence
KW  - Case-Control Studies
KW  - Child
KW  - Chromosome Breakage
KW  - Chromosome Deletion
KW  - Chromosomes, Artificial, Bacterial
KW  - Chromosomes, Human, Pair 16
KW  - DNA Primers
KW  - Female
KW  - Gene Frequency
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Male
KW  - Microsatellite Repeats
KW  - Pedigree
KW  - Phenotype
KW  - Polymerase Chain Reaction
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/hmg/ddm376
ER  -