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Article

Highlighted article: "identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse" by Stottmann, Bjork, Doyle, and Beier.

Genesis (New York, N.Y. : 2000) - 1 May 2010

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 20461822
DOI: 10.1002/dvg.20636

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Related research

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Research trail→

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Highlighted article: "identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse" by Stottmann, Bjork, Doyle, and Beier.PMID 20461822Read ↗

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Van der Woude syndrome: a review. Cardinal signs, epidemiology, associated features, differential diagnosis, expressivity, genetic counselling and treatment.Semantic proximity Read ↗

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Van der Woude syndrome: a report of two cases.Semantic proximity Read ↗

Van der Woude syndrome: a review of 11 cases seen at the Lagos University Teaching Hospital.Semantic proximity Read ↗

Van der Woude syndrome.Semantic proximity Read ↗

Waardenburg syndrome: variable phenotypic expression in monozygotic twins.Semantic proximity Read ↗

Towards a molecular understanding of cleft palate.Semantic proximity Read ↗

The mouse as a developmental model for cleft lip and palate research.Semantic proximity Read ↗

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