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p16 immunohistochemistry of multiple primary melanomas as screening to identify Familial Melanoma Syndrome
Author(s) -
Ponti Giovanni,
Luppi Gabriele,
Losi Lorena,
Cesinaro Anna Maria,
Sartori Giuliana,
Maiorana Antonio,
Pellacani Giovanni,
Longo Caterina,
Boni Elisa,
Pepe Patrizia,
Giannetti Alberto,
Seidenari Stefania,
Landi Maria Teresa
Publication year - 2012
Publication title -
international journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 93
eISSN - 1365-4632
pISSN - 0011-9059
DOI - 10.1111/j.1365-4632.2010.04496.x
Subject(s) - cdkn2a , immunohistochemistry , medicine , melanoma , pathology , mlh1 , fluorescence in situ hybridization , germline mutation , msh2 , cancer research , cancer , biology , mutation , gene , dna mismatch repair , genetics , colorectal cancer , chromosome
The Authors describe the use of p16 immunohistochemistry in multiple primary melanomas as screening to identify Familial Melanoma Syndrome