about
Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontiaAutism spectrum disorders: the quest for genetic syndromes.Intellectual Profiles in KBG-Syndrome: A Wechsler Based Case-Control Study.Partial deletion ofANKRD11results in the KBG phenotype distinct from the 16q24.3 microdeletion syndrome
P2860
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Twins with KBG syndrome and autism
@ast
Twins with KBG syndrome and autism
@en
type
label
Twins with KBG syndrome and autism
@ast
Twins with KBG syndrome and autism
@en
prefLabel
Twins with KBG syndrome and autism
@ast
Twins with KBG syndrome and autism
@en
P2093
P2860
P1476
Twins with KBG syndrome and autism
@en
P2093
Andrea D Torres
Jennifer M Phillips
Joachim F Hallmayer
Linda J Lotspeich
Sue C Cleveland
P2860
P2888
P304
P356
10.1007/S10803-009-0811-7
P407
P577
2009-07-14T00:00:00Z