Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders.
about
Identification of Developmental and Behavioral Markers Associated With Genetic Abnormalities in Autism Spectrum Disorder.Variable Penetrance of the 15q11.2 BP1-BP2 Microduplication in a Family with Cognitive and Language Impairment.Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population
P2860
Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Recurrent 15q11.2 BP1-BP2 micr ...... neurodevelopmental disorders.
@en
Recurrent 15q11.2 BP1-BP2 micr ...... neurodevelopmental disorders.
@nl
type
label
Recurrent 15q11.2 BP1-BP2 micr ...... neurodevelopmental disorders.
@en
Recurrent 15q11.2 BP1-BP2 micr ...... neurodevelopmental disorders.
@nl
prefLabel
Recurrent 15q11.2 BP1-BP2 micr ...... neurodevelopmental disorders.
@en
Recurrent 15q11.2 BP1-BP2 micr ...... neurodevelopmental disorders.
@nl
P2093
P2860
P356
P1476
Recurrent 15q11.2 BP1-BP2 micr ...... neurodevelopmental disorders.
@en
P2093
Antonio Maria Persico
Carla Lintas
Chiara Picinelli
Claudia Brogna
Roberto Sacco
Stefano Gabriele
P2860
P304
P356
10.1002/AJMG.B.32480
P577
2016-08-26T00:00:00Z