Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene.

Von Hippel-Lindau (VHL) disease is an autosomal dominant inherited familial cancer syndrome characterised by a predisposition to the development of retinal, cerebellar, and spinal haemangioblastomas, renal cell carcinoma, and phaeochromocytoma. The gene for VHL disease has been mapped to chromosome...

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Detalhes bibliográficos
Main Authors: Richards, F M, Maher, E R, Latif, F, Phipps, M E, Tory, K, Lush, M, Crossey, P A, Oostra, B, Enblad, P, Gustavson, K H
Formato: Artigo
Idioma:Inglês
Publicado em: 1993
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016263/
https://ncbi.nlm.nih.gov/pubmed/8445612
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