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Article

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

1 Feb 1993

Abstract excerpt

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 3p25-p26 and flanking markers identified. We report the detailed genetic mapping of the VHL disease locus in 38...

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Identifiers

PMID: 8445612
DOI: 10.1136/jmg.30.2.104

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