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Familial Cancer|May 11, 2005
SDHC mutations in hereditary paraganglioma/pheochromocytomaUlrich Müller, Christian Troidl, Stephan Niemann
Familial Cancer|May 11, 2005
Pheochromocytoma in von Hippel-Lindau disease and neurofibromatosis type 1Giuseppe Opocher, Pierantonio Conton, Francesca Schiavi, et al.
Familial Cancer|May 11, 2005
Imaging of pheochromocytoma and paragangliomaI Brink, S Hoegerle, J Klisch, et al.
Familial Cancer|July 5, 2006
Analysis of referrals to a multi-disciplinary breast cancer genetics clinic: practical and economic considerationsMarta M Reis, Dorothy Young, Lorna McLeish, et al.
Familial Cancer|December 13, 2005
MLH1 and MSH2 mutations in Colombian families with hereditary nonpolyposis colorectal cancer (Lynch syndrome)--description of four novel mutationsAlejandro Giraldo, Andrea Gómez, Gustavo Salguero, et al.
Familial Cancer|December 13, 2005
Behavioral and economic impact of a familial history of cancersFrancois Eisinger, Carole Tarpin, Laetitia Huiart, et al.
Familial Cancer|December 13, 2005
Linkage of a pedigree drawing program and database to a program for determining BRCA mutation carrier probabilitySharon R Sand, David S DeRam, Deborah J MacDonald, et al.
Familial Cancer|December 2, 2009
Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutationHanifa Bouzourene, Pierre Hutter, Lorena Losi, et al.
Familial Cancer|May 26, 2025
Pancreatic adenocarcinoma in a patient with a germline RB1 pathogenic variantRiya Patel, Christos Fountzilas, Michael Horowitz, et al.
Familial Cancer|May 26, 2025
Screening of biobank SNP-array genotyping data to detect Lynch syndrome predisposing MLH1 copy number variantsKimmo Ala-Kulju, Olli Carpén, Maarit Lappalainen, et al.
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