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AB110. The first prenatal diagnosis of von Hippel-Lindau syndrome in Chinese mainland
OBJECTIVE: Von Hippel-Lindau (VHL) syndrome is an autosomal dominantly inherited familial cancer syndrome caused by germline mutations in VHL tumor suppressor gene. It is characterized by multisystem neoplastic disorder which cannot be cured radically now, and the gold diagnosis standard is the gene...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
AME Publishing Company
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708671/ http://dx.doi.org/10.3978/j.issn.2223-4683.2015.s110 |