Rare syndromes of the head and face-Pierre Robin sequence.
about
A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.Bone morphogenetic protein type I receptor inhibition induces cleft palate associated with micrognathia and cleft lower lip in mice.High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development.
P2860
Rare syndromes of the head and face-Pierre Robin sequence.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Rare syndromes of the head and face-Pierre Robin sequence.
@en
Rare syndromes of the head and face-Pierre Robin sequence.
@nl
type
label
Rare syndromes of the head and face-Pierre Robin sequence.
@en
Rare syndromes of the head and face-Pierre Robin sequence.
@nl
prefLabel
Rare syndromes of the head and face-Pierre Robin sequence.
@en
Rare syndromes of the head and face-Pierre Robin sequence.
@nl
P2860
P356
P1476
Rare syndromes of the head and face-Pierre Robin sequence.
@en
P2093
Peter G Farlie
Tiong Yang Tan
P2860
P304
P356
10.1002/WDEV.69
P577
2012-05-14T00:00:00Z