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Familial Cancer|May 22, 2020
Low accuracy of self-reported family history of melanoma in high-risk patientsNicholas D Flint, Michael D Bishop, Tristan C Smart, et al.
Familial Cancer|June 7, 2020
Germline variants discovered in lymphoma patients undergoing tumor profiling: a case seriesAnthony J Scott, Molly C Tokaz, Michelle F Jacobs, et al.
Familial Cancer|September 14, 2021
A de novo pathogenic variant in the MSH6 gene in a 52 years-old womanElise Pierre-Noël, Fabrice Airaud, Estelle Cauchin, et al.
Familial Cancer|July 22, 2006
Low frequency of CHEK2 mutations in familial pancreatic cancerDetlef K Bartsch, Kristina Krysewski, Mercedes Sina-Frey, et al.
Familial Cancer|September 26, 2006
Surveillance and management of upper gastrointestinal disease in Familial Adenomatous PolyposisMichelle C Gallagher, Robin K S Phillips, Steffen Bulow
Familial Cancer|June 14, 2005
The Tyr978X BRCA1 mutation: occurrence in non-Jewish Iranians and haplotype in French-Canadian and non-Ashkenazi JewsLluís Quintana-Murci, Inbar Gal, Tangiz Bakhan, et al.
Familial Cancer|June 14, 2005
Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutationsAmy Østertun Geirdal, Jon G Reichelt, Alv A Dahl, et al.
Familial Cancer|June 14, 2005
An unusual case of Turcot's syndrome associated with ileal adenocarcinoma, intestinal non-Hodgkin's lymphoma, and duodenal adenocarcinoma. Review of the classification and genetic basis of Turcot's syndromeH R Murphy, W Taylor, A Ellis, et al.
Familial Cancer|June 14, 2005
Screening for exonic copy number mutations at MSH2 and MLH1 by MAPHSeyed Mohammad Akrami, Malcolm G Dunlop, Susan M Farrington, et al.
Familial Cancer|June 14, 2005
Informing one's family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory studyIlse Mesters, Marlein Ausems, Sophie Eichhorn, et al.
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