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Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 12, pp. e68 - e75
Journal Article
2015, ISBN 0444627022, Volume 132
von Hippel–Lindau (VHL) disease is an inheritable condition with an incidence of 1 in 36 000 live births. Individuals with VHL develop benign and malignant... 
clear cell renal cell carcinoma | von Hippel Lindau disease | endolymphatic sac tumor | ELST | hemangioblastoma | VHL | second hit | pVHL | Clear cell renal cell carcinoma | Endolymphatic sac tumor | Second hit | Von Hippel Lindau disease | Hemangioblastoma | PVHL | von Hippel-Lindau Disease - genetics | Humans | von Hippel-Lindau Disease - epidemiology
Book Chapter
European Journal of Human Genetics, ISSN 1018-4813, 02/2017, Volume 25, Issue 3, pp. 301 - 307
Journal Article
Radiologic Clinics of North America, ISSN 0033-8389, 05/2016, Volume 54, Issue 3, pp. 409 - 422
Journal Article
Journal Article
Clinical Genetics, ISSN 0009-9163, 01/2010, Volume 77, Issue 1, pp. 49 - 59
Poulsen MLM, Budtz-Jørgensen E, Bisgaard ML. Surveillance in von Hippel-Lindau disease (vHL).von Hippel-Lindau disease (vHL) is a hereditary multisystem cancer... 
renal cell carcinoma | retinal hemangioma | central nervous system hemangioblastoma | prophylactic surveillance | von Hippel-Lindau disease | von Hippel‐Lindau disease | Prophylactic surveillance | Central nervous system hemangioblastoma | Renal cell carcinoma | Retinal hemangioma | Von Hippel-Lindau disease | MOLECULAR-GENETIC ANALYSIS | TUMOR-SUPPRESSOR GENE | PARENTS | CEREBELLAR HEMANGIOBLASTOMA | NATURAL-HISTORY | RENAL-CELL CARCINOMA | CLINICAL MANAGEMENT | IMAGING FEATURES | GENETICS & HEREDITY | GERMLINE MUTATIONS | CENTRAL-NERVOUS-SYSTEM | Central Nervous System Diseases - genetics | Retinal Diseases - genetics | Humans | Middle Aged | Male | Retinal Diseases - epidemiology | Incidence | von Hippel-Lindau Disease - diagnosis | Young Adult | Hemangioblastoma - epidemiology | Adult | Female | Von Hippel-Lindau Tumor Suppressor Protein - genetics | Child | Hemangioma - genetics | Retinal Diseases - diagnosis | Central Nervous System Diseases - epidemiology | von Hippel-Lindau Disease - epidemiology | Hemangioblastoma - diagnosis | Hemangioma - epidemiology | von Hippel-Lindau Disease - genetics | Hemangioma - diagnosis | Hemangioblastoma - genetics | Adolescent | Denmark - epidemiology | Heterozygote | Central Nervous System Diseases - diagnosis | Early Diagnosis | Population Surveillance | Medical records | Genetic disorders | Disease management | Risk factors | Cancer
Journal Article
Journal Article
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 04/2012, Volume 57, Issue 4, pp. 238 - 243
Von Hippel-Lindau (VHL) disease is an autosomal dominant familial cancer syndrome caused by germline mutations in VHL tumor suppressor gene. It is... 
de novo mutation | mutation | Chinese | renal cell carcinoma |