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

Identification of the von Hippel-Lindau Disease Tumor Suppressor Gene

1993 • 2,906 citations

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A

1993 • 1,941 citations

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

1994 • 1,140 citations

Clinical Features and Natural History of von Hippel-Lindau Disease

1990 • 916 citations

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

1994 • 646 citations

Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours

1994 • 531 citations

Identification of intragenic mutations in the Von Hippel — Lindau disease tumour suppressor gene andcorrelation with disease phenotype

1994 • 386 citations

A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC.

1995 • 253 citations

Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect

1995 • 177 citations

A Practical Guide to Human Cancer Genetics

2006 • 87 citations

10 Multiple endocrine neoplasia

1988 • 54 citations

Genetic linkage between Von Hippel—Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus

1993 • 52 citations

A Practical Guide to Human Cancer Genetics

1994 • 24 citations

A polymorphic dinucleotide repeat at the ZNF22 locus.

1993 • 15 citations

Familial risk for neuroendocrine tumors.

1993 • 14 citations

A polymorphic dinucleotide repeat at the D10S141 locus

1993 • 9 citations