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Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT
Cancer Risks for PMS2-Associated Lynch Syndrome