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European Journal of Human Genetics, ISSN 1018-4813, 06/2011, Volume 19, Issue 6, pp. 617 - 623
The autosomal dominantly inherited disorder von Hippel-Lindau disease (VHL) is caused by germline mutations in the VHL tumour suppressor gene (TSG). VHL... 
renal cysts | phaeochromocytoma | renal carcinoma | VHL | von Hippel-Lindau | haemangioblastoma | SPARING SURGERY | GENOTYPE-PHENOTYPE CORRELATIONS | BIOCHEMISTRY & MOLECULAR BIOLOGY | TUMOR-SUPPRESSOR GENE | ENDOCRINE NEOPLASIA TYPE-2 | NATURAL-HISTORY | RETINAL HEMANGIOBLASTOMA | RENAL-CELL CARCINOMA | RECEPTOR INHIBITOR SU5416 | GENETICS & HEREDITY | CENTRAL-NERVOUS-SYSTEM | ENDOLYMPHATIC SAC TUMORS | Genetic Predisposition to Disease | Carcinoma, Renal Cell - pathology | Pheochromocytoma - diagnosis | Pheochromocytoma - etiology | Hemangioblastoma - etiology | Humans | Carcinoma, Renal Cell - genetics | Hemangioblastoma - diagnosis | von Hippel-Lindau Disease - complications | von Hippel-Lindau Disease - genetics | von Hippel-Lindau Disease - diagnosis | Magnetic Resonance Imaging | von Hippel-Lindau Disease - pathology | Hemangioblastoma - pathology | Mass Screening | Genes, Dominant | Hemangioblastoma - genetics | Carcinoma, Renal Cell - diagnosis | Germ-Line Mutation | Pheochromocytoma - pathology | Pheochromocytoma - genetics | Von Hippel-Lindau Tumor Suppressor Protein - genetics | Adrenal Gland Neoplasms | Carcinoma, Renal Cell - etiology | Biomedical research | Medical imaging | Central nervous system | Retina | Nervous system | Family medical history | Preventive medicine | Patients | Von Hippel-Lindau disease | Reviews | Cysts | Genetics | VHL protein | Mutation | Neoplasia | Clear cell-type renal cell carcinoma | Cancer | Tumors | Practical Genetics | von Hippel–Lindau
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