Associated Papers
Comprehensive analysis of the functional impact of single nucleotide variants of human CHEK2.
McCarthy-Leo CE et al.
Plos Genetics, 2024
39146382 (PubMed )
Supplement: pgen.1011375.s008.xlsx › All_SNVs_Data
Germline Mutation Analysis in Sporadic Breast Cancer Cases With Clinical Correlations.
Ajaz S et al.
Frontiers in Genetics, 2022
Genetics of breast cancer in African populations: a literature review.
Abbad A et al.
Global Health, Epidemiology and Genomics, 2018
Novel Nonsense Variants c.58C>T (p.Q20X) and c.256G>T (p.E85X) in the CHEK2 Gene Identified dentified in Breast Cancer Patients from Balochistan.
Baloch AH et al.
Asian Pacific Journal of Cancer Prevention : Apjcp, 2016
Novel Nonsense Variants c.58C>T (p.Q20X) and c.256G>T (p.E85X) in the CHEK2 Gene Identified in Breast Cancer Patients from Balochistan.
Baloch AH et al.
Asian Pacific Journal of Cancer Prevention : Apjcp, 2016
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