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Van der Woude syndrome- a syndromic form of orofacial clefting
Van der Woude Syndrome is the most common form of syndromic orofacial clefting, accounting for 2% of all cases, and has the phenotype that most closely resembles the more common non-syndromic forms. The syndrome has an autosomal dominant hereditary pattern with variable expressivity and a high degre...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medicina Oral S.L.
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3908796/ https://ncbi.nlm.nih.gov/pubmed/24558537 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4317/jced.50559 |
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