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(1 - 11 of 11)
High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations
International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer
Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome
Indication for CDKN2A-mutation analysis in familial pancreatic cancer families without melanomas
Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study
Body weight and risk of breast cancer in BRCA1/2 mutation carriers
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes
Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences
Body weight and risk of breast cancer in BRCA1/2 mutation carriers