TY  - GEN
AU  - Ching,Michael S L
AU  - Shen,Yiping
AU  - Tan,Wen-Hann
AU  - Jeste,Shafali S
AU  - Morrow,Eric M
AU  - Chen,Xiaoli
AU  - Mukaddes,Nahit M
AU  - Yoo,Seung-Yun
AU  - Hanson,Ellen
AU  - Hundley,Rachel
AU  - Austin,Christina
AU  - Becker,Ronald E
AU  - Berry,Gerard T
AU  - Driscoll,Katherine
AU  - Engle,Elizabeth C
AU  - Friedman,Sandra
AU  - Gusella,James F
AU  - Hisama,Fuki M
AU  - Irons,Mira B
AU  - Lafiosca,Tina
AU  - LeClair,Elaine
AU  - Miller,David T
AU  - Neessen,Michael
AU  - Picker,Jonathan D
AU  - Rappaport,Leonard
AU  - Rooney,Cynthia M
AU  - Sarco,Dean P
AU  - Stoler,Joan M
AU  - Walsh,Christopher A
AU  - Wolff,Robert R
AU  - Zhang,Ting
AU  - Nasir,Ramzi H
AU  - Wu,Bai-Lin
TI  - Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders
SN  - 1552-485X
PY  - 2010///0903
KW  - Autistic Disorder
KW  - genetics
KW  - Child
KW  - Child Development Disorders, Pervasive
KW  - Comparative Genomic Hybridization
KW  - Developmental Disabilities
KW  - Female
KW  - Humans
KW  - Intellectual Disability
KW  - Language Development Disorders
KW  - Male
KW  - Mutation
KW  - Phenotype
KW  - Schizophrenia
KW  - Sequence Deletion
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.b.31063
ER  -