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Article

Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in the ZEB2 gene.

American journal of medical genetics. Part A - 1 Dec 2008

Cecconi Massimiliano, Forzano Francesca, Garavelli Livia, Pantaleoni Chiara, Grasso Marina, Dagna Bricarelli Franca, Perroni Lucia, Di Maria Emilio, Faravelli Francesca

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Identifiers

PMID: 19006215
DOI: 10.1002/ajmg.a.32568

Genes

ZEB2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in the ZEB2 gene.PMID 19006215Read ↗

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Mowat–Wilson syndrome: an underdiagnosed syndrome?Semantic proximity Read ↗

Mowat–Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular InteractionsSemantic proximity Read ↗

[Analysis of a case with Mowat-Wilson syndrome caused by ZEB2 gene variant].Semantic proximity Read ↗

Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS).Semantic proximity Read ↗

Mowat-Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity.Semantic proximity Read ↗

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Mowat-Wilson syndrome.Semantic proximity Read ↗

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