Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2.
about
Posterior polymorphous corneal dystrophy 3 is associated with agenesis and hypoplasia of the corpus callosumLoss of Sip1 leads to migration defects and retention of ectodermal markers during lens development.Hirschsprung's disease in children with Mowat-Wilson syndrome.A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson Syndrome.ZEB2 gene mutation and duplication of 22q11.23 in Mowat-Wilson syndrome.Clinical spectrum of eye malformations in four patients with Mowat-Wilson syndrome.CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases
P2860
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P2860
Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2.
@en
type
label
Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2.
@en
prefLabel
Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2.
@en
P2093
P2860
P1433
P1476
Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2.
@en
P2093
Elias I Traboulsi
Kristina Natan
Michelle Ariss
Neil Friedman
P2860
P304
P356
10.3109/13816810.2011.610860
P577
2012-04-09T00:00:00Z