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Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma–pancreatic carcinoma–prone families : The familial atypical multiple mole melanoma–pancreatic carcinoma syndrome

✍ Scribed by Henry T. Lynch; Randall E. Brand; David Hogg; Carolyn A. Deters; Ramon M. Fusaro; Jane F. Lynch; Ling Liu; Joseph Knezetic; Norman J. Lassam; Michael Goggins; Scott Kern

Publisher: John Wiley and Sons
Year: 2001
Tongue: English
Weight: 188 KB
Volume: 94
Category: Article
ISSN: 0008-543X
DOI: 10.1002/cncr.10159

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## Abstract ## BACKGROUND Previous studies suggest that the familial atypical multiple‐mole melanoma (FAMMM) syndrome may predispose affected families to nonmelanoma carcinomas, including adenocarcinoma of the pancreas. It has been found that many of these families harbor mutations in the __CDKN2A