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Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 gene
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers
Do preferred risk formats lead to better understanding?
Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy
CDC73-Related Disorders: Clinical Manifestations and Case Detection in Primary Hyperparathyroidism
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers
Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
Low penetrance of paraganglioma and pheochromocytoma in an extended kindred with a germline SDHB exon 3 deletion
Lynch Syndrome Caused by Germline PMS2 Mutations: Delineating the Cancer Risk
Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D)
Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists
The effectiveness of a graphical presentation in addition to a frequency format in the context of familial breast cancer risk communication: a multicenter controlled trial
Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome
Genetic counseling does not fulfill the counselees' need for certainty in hereditary breast/ovarian cancer families: an explorative assessment
The counselees' self-reported request for psychological help in genetic counseling for hereditary breast/ovarian cancer: not only psychopathology matters
Opening the psychological black box in genetic counseling. The psychological impact of DNA testing is predicted by the counselees' perception, the medical impact by the pathogenic or uninformative BRCA1/2-result
Exploring the short-term impact of DNA-testing in breast cancer patients: The counselees' perception matters, but the actual BRCA1/2 result does not
Perceiving cancer-risks and heredity-likelihood in genetic-counseling: how counselees recall and interpret BRCA1/2-test results
Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
Childhood Brain Tumours Due To Germline Bi-Allelic Mismatch Repair Gene Mutations
Perceiving cancer-risks and heredity-likelihood in genetic-counseling: how counselees recall and interpret BRCA 1/2-test results
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes