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

BACKGROUND Hereditary pancreatic carcinoma shows extant phenotypic and genotypic heterogeneity as evidenced by its integral association with a variety of hereditary cancer syndromes inclusive of the familial atypical multiple mole melanoma (FAMMM) syndrome in concert with CDKN2A (p16) germline mutat...

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Veröffentlicht in:Cancer 2002-01, Vol.94 (1), p.84-96
Hauptverfasser: Lynch, Henry T., Brand, Randall E., Hogg, David, Deters, Carolyn A., Fusaro, Ramon M., Lynch, Jane F., Liu, Ling, Knezetic, Joseph, Lassam, Norman J., Goggins, Michael, Kern, Scott
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