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Velthuizen, M.E.
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Ausems, M.G.E.M.
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Vasen, H.F.A.
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Asperen, C.J. van
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Estimated prevalence, tumor spectrum, and neurofibromatosis type 1-like phenotype of CDKN2A-related melanoma-astrocytoma syndrome
Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer
Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing
Identification and management of Lynch syndrome in the Middle East and North African countries
Increased prevalence of Barrett's esophagus in patients with MUTYH-associated polyposis (MAP)
Increased prevalence of Barrett's esophagus in patients with MUTYH-associated polyposis (MAP)
TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort
Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry
Lynch Syndrome Caused by Germline PMS2 Mutations: Delineating the Cancer Risk
Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations