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9. Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden). Vasen HF; Gruis NA; Frants RR; van Der Velden PA; Hille ET; Bergman W Int J Cancer; 2000 Sep; 87(6):809-11. PubMed ID: 10956390 [TBL] [Abstract][Full Text] [Related]
11. Development of esophageal squamous cell cancer in patients with FAMMM syndrome: Two clinical reports. van der Wilk BJ; Noordman BJ; Atmodimedjo PN; Dinjens WNM; Laheij RJF; Wagner A; Wijnhoven BPL; van Lanschot JJB Eur J Med Genet; 2020 Mar; 63(3):103840. PubMed ID: 31923587 [TBL] [Abstract][Full Text] [Related]
12. The absence of multiple atypical nevi in germline CDKN2A mutations: Comment on "Hereditary melanoma: Update on syndromes and management: Genetics of familial atypical multiple mole melanoma syndrome". Ipenburg NA; Gruis NA; Bergman W; van Kester MS J Am Acad Dermatol; 2016 Oct; 75(4):e157. PubMed ID: 27646763 [No Abstract] [Full Text] [Related]