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Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
Cancer Risks for PMS2-Associated Lynch Syndrome
Identification and comprehensive characterization of large genomic rearrangements in the BRCA1 and BRCA2 genes.
Detection of APC gene deletions using quantitative multiplex PCR of short fluorescent fragments
