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Autor:
Holger Hummerich, Susanne C. Szymanski, Elisabeth Schröder, Michael I. Lerman, G. Röhrborn, Farida Latif
Publikováno v:
Human genetics. 92(3)
Von Hippel-Lindau disease is a heritable tumour syndrome caused by the loss of the function of a tumour suppressor gene on the short arm of human chromosome 3. The interval RAF1-D3S18 (3p25–3p26) has been identfied by genetic linkage studies to har
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b12952f077bfa9eeadf269cf4eecc3ad
https://pubmed.ncbi.nlm.nih.gov/8406436
https://pubmed.ncbi.nlm.nih.gov/8406436
