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干扰素调节因子6基因致病的Van der Woude综合征的家系调查和遗传特点分析
OBJECTIVE: This study aimed to investigate the clinical phenotype and genetic characteristics of Chinese families with Van der Woude syndrome (VWS). METHODS: Clinical manifestations between 14 families and within each family were recorded. Possible inheritance modes and pathogenic genes were analyze...
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| Publicado no: | Hua Xi Kou Qiang Yi Xue Za Zhi |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
华西口腔医学杂志编辑部
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7039798/ https://ncbi.nlm.nih.gov/pubmed/30593107 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7518/hxkq.2018.06.008 |
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