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Familial Cancer|October 31, 2026
Double heterozygous pathogenic germline APC and MSH2 variants in a 16-year-old female diagnosed with colorectal cancerElena Maccaroni, Riccardo Bacalini, Alessia Lancianese, et al.
Familial Cancer|October 14, 2010
Genetic epidemiological analysis reveals a multi-gene additive model for gastric cancerSanyou Gao, Xiaohui Zhang, Peng Wang, et al.
Familial Cancer|December 29, 2010
Case report: renal cell carcinoma segregating with a t(2;3)(q37.3;q13.2) chromosomal translocation in an Ashkenazi Jewish familyL McKay, M Frydenberg, L Lipton, et al.
Familial Cancer|December 29, 2010
Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastomaIngrid Slade, Anne Murray, Sandra Hanks, et al.
Familial Cancer|December 15, 2010
Mutation analysis of the PALB2 cancer predisposition gene in familial melanomaN Sabbaghian, R Kyle, A Hao, et al.
Familial Cancer|November 10, 2010
Strictly defined familial male breast cancerUwe Güth, Dieter Müller, Dorothy Jane Huang, et al.
Familial Cancer|December 8, 2010
The impact of cancer pathology confirmation on clinical management of a family history of cancerE Edwards, A Lucassen
Familial Cancer|November 13, 2010
Lack of GNAQ germline mutations in uveal melanoma patients with high risk for hereditary cancer predispositionMohamed H Abdel-Rahman, Robert Pilarski, James B Massengill, et al.
Familial Cancer|July 20, 2010
Lynch syndrome: the influence of environmental factors on extracolonic cancer risk in hMLH1 c.C1528T mutation carriers and their mutation-negative sistersM M Blokhuis, G E Pietersen, P A Goldberg, et al.
Familial Cancer|July 20, 2010
MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversionsJérémie H Lefevre, Chrystelle Colas, Florence Coulet, et al.
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