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Familial Cancer|February 13, 2020
Missense PALB2 germline variant disrupts nuclear localization of PALB2 in a patient with breast cancerMing Ren Toh, Chen Ee Low, Siao Ting Chong, et al.Familial Cancer|February 8, 2019
Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care SettingElizabeth V Clarke, Kristin R Muessig, Jamilyn Zepp, et al.Familial Cancer|November 28, 2018
Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndromeShahid Mahmood Baig, Ambrin Fatima, Muhammad Tariq, et al.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.Pageof 152