Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma.

Inherited predisposition to phaeochromocytoma is seen in multiple endocrine neoplasia type 2 syndromes, von Hippel-Lindau (VHL) disease, and neuro-fibromatosis type 1. In addition familial phaeochromocytoma alone has been reported. To investigate the genetic basis for familial phaeochromocytoma alon...

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Bibliografski detalji
Glavni autori: Crossey, P A, Eng, C, Ginalska-Malinowska, M, Lennard, T W, Wheeler, D C, Ponder, B A, Maher, E R
Format: Artigo
Jezik:Inglês
Izdano: 1995
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051741/
https://ncbi.nlm.nih.gov/pubmed/8592333
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