about
A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasiaIdentification of novel ROR2 gene mutations in Indian children with Robinow syndrome.A Novel de novo FZD2 Mutation in a Patient with Autosomal Dominant Omodysplasia.Two unrelated patients with autosomal dominant omodysplasia and mutations
P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Omodysplasia: an affected mother and son.
@ast
Omodysplasia: an affected mother and son.
@en
Omodysplasia: an affected mother and son.
@nl
type
label
Omodysplasia: an affected mother and son.
@ast
Omodysplasia: an affected mother and son.
@en
Omodysplasia: an affected mother and son.
@nl
prefLabel
Omodysplasia: an affected mother and son.
@ast
Omodysplasia: an affected mother and son.
@en
Omodysplasia: an affected mother and son.
@nl
P2093
P2860
P356
P1476
Omodysplasia: an affected mother and son.
@en
P2093
Charles P Venditti
Christopher A Friedrich
Craig Alter
Deborah A Driscoll
Elaine H Zackai
Jennifer Farmer
Karen L Russell
Linton Whitaker
Michael T Mennuti
P2860
P304
P356
10.1002/AJMG.10555
P577
2002-08-01T00:00:00Z