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Clinical review of genetic epileptic encephalopathiesNeuroimaging findings in Mowat-Wilson syndrome: a study of 54 patientsHirschsprung's disease in children with Mowat-Wilson syndrome.Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples.
P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Clinical utility gene card for: Mowat-Wilson syndrome
@en
type
label
Clinical utility gene card for: Mowat-Wilson syndrome
@en
prefLabel
Clinical utility gene card for: Mowat-Wilson syndrome
@en
P2093
P2860
P356
P1476
Clinical utility gene card for: Mowat-Wilson syndrome
@en
P2093
Anita Rauch
Livia Garavelli
Marcella Zollino
P2860
P2888
P304
P356
10.1038/EJHG.2011.12
P577
2011-02-23T00:00:00Z