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A Case of Vander Woude Syndrome with Rare Phenotypic Expressions
Van der Woude syndrome (VWS) is a rare developmental disorder with an autosomal dominant inheritance. The prevalence of VWS varies from 1:100,000 to 1:40,000 still born or live births. It has variable expressivity and generally expressed as orofacial manifestations like lower lip pits, cleft lip and...
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| Publicado no: | J Clin Diagn Res |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
JCDR Research and Publications (P) Limited
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4253239/ https://ncbi.nlm.nih.gov/pubmed/25478421 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2014/10420.5008 |
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