about
Compound heterozygous alterations in intraflagellar transport protein CLUAP1 in a child with a novel Joubert and oral-facial-digital overlap syndromeMotile and non-motile cilia in human pathology: from function to phenotypes.Mechanisms for nonmitotic activation of Aurora-A at cilia.Oral-facial-digital syndrome type 1 in males: Congenital heart defects are included in its phenotypic spectrum.Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes.Loss of Tctn3 causes neuronal apoptosis and neural tube defects in mice.
P2860
description
2016 nî lūn-bûn
@nan
2016 թուականին հրատարակուած գիտական յօդուած
@hyw
2016 թվականին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Update on oral-facial-digital syndromes (OFDS)
@ast
Update on oral-facial-digital syndromes (OFDS)
@en
Update on oral-facial-digital syndromes (OFDS)
@nl
type
label
Update on oral-facial-digital syndromes (OFDS)
@ast
Update on oral-facial-digital syndromes (OFDS)
@en
Update on oral-facial-digital syndromes (OFDS)
@nl
prefLabel
Update on oral-facial-digital syndromes (OFDS)
@ast
Update on oral-facial-digital syndromes (OFDS)
@en
Update on oral-facial-digital syndromes (OFDS)
@nl
P2860
P3181
P1433
P1476
Update on oral-facial-digital syndromes (OFDS)
@en
P2860
P2888
P3181
P356
10.1186/S13630-016-0034-4
P407
P577
2016-01-01T00:00:00Z
P6179
1028684818