المؤلفون: Hartmut P. H. Neumann, Jörg Laubenberger, Manfred Olschewski, Dieter Schmidt, Günter Kirste, Bernhard U. Bender, Carsten Altehöfer, Dietmar P. Berger, Charis Eng, Henning Miosczka, Miro Orszagh, Vera Van Velthoven

المصدر: Journal of medical genetics. 38(8)

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Angiomatosis, von Hippel-Lindau Disease, endocrine system diseases, Adolescent, Ubiquitin-Protein Ligases, Population, DNA Mutational Analysis, Penetrance, Pheochromocytoma, urologic and male genital diseases, Gastroenterology, Ligases, Germline mutation, Internal medicine, Hemangioblastoma, Genetics, medicine, Humans, Point Mutation, Cumulative incidence, Von Hippel–Lindau disease, education, Child, Survival rate, Genetics (clinical), Aged, Aged, 80 and over, education.field_of_study, business.industry, Mortality rate, Tumor Suppressor Proteins, Age Factors, Original Articles, Middle Aged, medicine.disease, Survival Analysis, female genital diseases and pregnancy complications, Survival Rate, Endocrinology, Von Hippel-Lindau Tumor Suppressor Protein, Child, Preschool, Female, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdf977e2df61b291dadc2fe8b237b7d1
https://pubmed.ncbi.nlm.nih.gov/11483638