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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 LucassenFamilial 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.Familial Cancer|July 13, 2010
Pancreatic cancer risk counselling and screening: impact on perceived risk and psychological functioningChristine Maheu, Andrea Vodermaier, Heidi Rothenmund, et al.Familial Cancer|September 21, 2010
A whisper-game perspective on the family communication of DNA-test results: a retrospective study on the communication process of BRCA1/2-test results between proband and relativesJoël Vos, Fred Menko, Anna M Jansen, et al.Familial Cancer|September 21, 2010
Communicating genetic risk information within families: a reviewMel Wiseman, Caroline Dancyger, Susan MichiePageof 151