Κυριακή 6 Φεβρουαρίου 2022

Hereditary oral squamous cell carcinoma associated with CDKN2A germline mutation: a case report

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Germline CDKN2A mutations are a well-known cause of familial atypical multiple mole melanoma (OMIM #155601) and melanoma-pancreatic cancer syndrome (OMIM #606719). Increased risk of head and neck squamous cell ca...
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