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Familial Cancer|January 23, 2020
Neurofibromatosis type 2 discordance in monozygous twinsS Amico, P Smith, S Tobi, et al.
Familial Cancer|September 11, 2020
Worldwide variation in lynch syndrome screening: case for universal screening in low colorectal cancer prevalence areasGeorge Kunnackal John, Vipin Das Villgran, Christine Caufield-Noll, et al.
Familial Cancer|September 2, 2005
Frequency of familial colon cancer and hereditary nonpolyposis colorectal cancer (Lynch syndrome) in a large population databaseRichard A Kerber, Deborah W Neklason, Wade S Samowitz, et al.
Familial Cancer|June 14, 2005
High prevalence of two BRCA1 mutations, 4154delA and 5382insC, in LatviaLaima Tikhomirova, Olga Sinicka, Dagnija Smite, et al.
Familial Cancer|June 14, 2005
The CHEK2 1100delC allele is not relevant for risk assessment in HNPCC and HBCC Spanish familiesAna Sánchez de Abajo, Miguel de la Hoya, Javier Godino, et al.
Familial Cancer|March 11, 2006
The value of multi-modal gene screening in HNPCC in Quebec: three mutations in mismatch repair genes that would have not been correctly identified by genomic DNA sequencing aloneSusan McVety, Lili Li, Isabelle Thiffault, et al.
Familial Cancer|May 11, 2005
Molecular pathogenesis of MEN2-associated tumorsChristian A Koch
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.
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