about
Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiologyNeurobehavioral Alterations in a Genetic Murine Model of Feingold Syndrome 2MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia.Identification of disease genes by whole genome CGH arrays.
P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Familial syndromic esophageal atresia maps to 2p23-p24
@nl
Familial syndromic esophageal atresia maps to 2p23-p24.
@ast
Familial syndromic esophageal atresia maps to 2p23-p24.
@en
type
label
Familial syndromic esophageal atresia maps to 2p23-p24
@nl
Familial syndromic esophageal atresia maps to 2p23-p24.
@ast
Familial syndromic esophageal atresia maps to 2p23-p24.
@en
prefLabel
Familial syndromic esophageal atresia maps to 2p23-p24
@nl
Familial syndromic esophageal atresia maps to 2p23-p24.
@ast
Familial syndromic esophageal atresia maps to 2p23-p24.
@en
P2093
P2860
P356
P1476
Familial syndromic esophageal atresia maps to 2p23-p24
@en
P2093
Brunner HG
Govaerts LC
Hennekam RC
Kingston H
P2860
P304
P356
10.1086/302779
P407
P577
2000-02-01T00:00:00Z