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Kidney cancer in the Swedish Family Cancer Database: familial risks and second primary malignancies
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype
Risk of second cancer among women with breast cancer
Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer
Polyglutamine repeat length in the NCOA3 does not affect risk in familial breast cancer
Trisomy 8q and partial trisomy 22 in a 43-year-old man with moderate intellectual disability, epilepsy and large cell non-Hodgkin lymphoma
Aurora kinases A and B and familial breast cancer risk
Sex hormone-binding globulin polymorphisms in familial and sporadic breast cancer
MTHFR and MTRR genotype and haplotype analysis and colorectal cancer susceptibility in a case–control study from the Czech Republic
