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Familial Cancer|May 8, 2004
Cancer variation associated with the position of the mutation in the BRCA2 geneJan Lubinski, Catherine M Phelan, Parviz Ghadirian, et al.Familial Cancer|September 2, 2004
HNPCC and sporadic MSI-H colorectal cancer: a review of the morphological similarities and differencesJeremy R JassFamilial Cancer|September 2, 2004
Correlations between phenotype and microsatellite instability in HNPCC: implications for genetic testingRaffaele Palmirotta, Sabino Matera, Maria Cristina Curia, et al.Familial Cancer|October 24, 2009
An Ashkenazi founder mutation in the MSH6 gene leading to HNPCCYael Goldberg, Rinnat M Porat, Inbal Kedar, et al.Familial Cancer|December 8, 2009
Female BRCA mutation carriers with a preference for prophylactic mastectomy are more likely to participate an educational-support group and to proceed with the preferred intervention within 2 yearsKarin M Landsbergen, Judith B Prins, Yvonne J L Kamm, et al.Familial Cancer|December 2, 2009
Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/2 mutation detectionJ J T van Harssel, C E P van Roozendaal, Y Detisch, et al.Familial Cancer|December 13, 2005
Mutational analysis of hMsh6 in Israeli HNPCC and HNPCC-like familiesShiri Dovrat, Arie Figer, Herma H Fidder, et al.Familial Cancer|December 13, 2005
Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening proceduresAnja Wagner, Ingrid van Kessel, Mieke G Kriege, et al.Familial Cancer|December 13, 2005
Neurofibromatosis 2 (NF2) and malignant mesothelioma in a man with a constitutional NF2 missense mutationM E Baser, H Rai, A J Wallace, et al.Familial Cancer|December 13, 2005
Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutationsPrathap BandipalliamPageof 152