Associated Papers
Phenotypic evaluation of deep learning models for classifying germline variant pathogenicity.
Chow RD et al.
Npj Precision Oncology, 2024
39427061 (PubMed )
Supplement: 41698_2024_710_MOESM2_ESM.xlsx › S3
Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer.
Landwehr R et al.
Breast Cancer Research and Treatment, 2011
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