Amal Yussuf
0000-0002-7876-2713
4 papers found
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Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C
Development and Validation of the PREMMplus Model for Multigene Hereditary Cancer Risk Assessment
Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast
Risk of Late-Onset Breast Cancer in Genetically Predisposed Women
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