SCOPUS 정보 검색 플랫폼

Volumn 87, Issue 6, 2000, Pages 809-811

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden)

(6) Vasen, H F A a,b Gruis, N A b Frants, R R b Van Der Velden, P A b Hille, E T M b Bergman, W b

a Foundation for the Detection of Hereditary Tumours (Netherlands)

b LEIDEN UNIVERSITY MEDICAL CENTER (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN P16;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CANCER EPIDEMIOLOGY; CANCER RISK; CANCER SUSCEPTIBILITY; DISEASE ASSOCIATION; EXON; GENE DELETION; HUMAN; MAJOR CLINICAL STUDY; MELANOMA; MUTATION; PANCREAS CANCER; PRIORITY JOURNAL;

ADULT; AGE FACTORS; AGED; CYCLIN-DEPENDENT KINASE INHIBITOR P16; DYSPLASTIC NEVUS SYNDROME; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LUNG NEOPLASMS; MALE; MIDDLE AGED; NETHERLANDS; PANCREATIC NEOPLASMS; RETROSPECTIVE STUDIES; RISK; SKIN NEOPLASMS;

EID: 0033836334 PISSN: 00207136 EISSN: None Source Type: Journal
DOI: 10.1002/1097-0215(20000915)87:6<809::AID-IJC8>3.0.CO;2-U Document Type: Article

Times cited : (351)

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