Associated Papers
Comprehensive Analysis of 15 Cases of ELOC -RCC and Identification of Novel Mutation Site.
Wu Y et al.
The American Journal of Surgical Pathology, 2025
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
A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene.
Fierheller CT et al.
Genome Medicine, 2021
34861889 (PubMed )
Supplement: 13073_2021_998_MOESM1_ESM.xlsx › S9
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