Associated Papers
Understanding and predicting the functional consequences of missense mutations in BRCA1 and BRCA2.
Aljarf R et al.
Scientific Reports, 2022
35729312 (PubMed )
Supplement: 41598_2022_13508_MOESM2_ESM.xlsx › Sheet1
Analysis of sequence variants in the 3'UTR of CDKN2A gene in melanoma patients.
Przybyła A et al.
Contemporary Oncology (poznan, Poland), 2015
Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish population.
Loo JC et al.
Journal of Medical Genetics, 2005
Two p16 (CDKN2A) germline mutations in 30 Israeli melanoma families.
Yakobson E et al.
European Journal of Human Genetics : Ejhg, 2000
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