CDKN2A Germline Mutations in U.K. Patients with Familial Melanoma and Multiple Primary Melanomas
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
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1. CDKN2A germline alterations and the relevance of genotype-phenotype associations in cancer predisposition;Hereditary Cancer in Clinical Practice;2021-03-25
2. Multiple primary cutaneous melanomas: recent studies highlight features associated with more indolent behaviour;Pathology;2013-01
3. Familial melanoma: Clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family;Journal of the American Academy of Dermatology;2012-12
4. The CDKN2A G500 Allele Is More Frequent in GBM Patients with No Defined Telomere Maintenance Mechanism Tumors and Is Associated with Poorer Survival;PLoS ONE;2011-10-26
5. Significance of CDKN2A gene A148T variant in patients with bladder cancer;Central European Journal of Urology;2011
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