Associated Papers
Whole-exome sequencing for identification of specific gene mutations in an Indian cohort of triple-negative breast cancer patients.
Preeti P et al.
Discover Oncology, 2025
41324770 (PubMed )
Supplement: 12672_2025_3921_MOESM2_ESM.xlsx › Sheet1
Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles.
Thompson ER et al.
Plos Genetics, 2012
23028338 (PubMed )
Supplement: pgen.1002894.s003.xlsx › Table_S2_Exome_variants
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