Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414.

Van der Woude syndrome (VWS) is an autosomal dominant craniofacial disorder characterized by lip pits, clefting of the primary or secondary palate, and hypodontia. The gene has been localized, by RFLP-based linkage studies, to region 1q32-41 between D1S65-REN and D1S65-TGFB2. In this study we report...

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Detalhes bibliográficos
Main Authors: Sander, A, Murray, J C, Scherpbier-Heddema, T, Buetow, K H, Weissenbach, J, Zingg, M, Ludwig, K, Schmelzle, R
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801300/
https://ncbi.nlm.nih.gov/pubmed/7825592
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