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Familial Cancer|June 14, 2005
Screening for exonic copy number mutations at MSH2 and MLH1 by MAPHSeyed Mohammad Akrami, Malcolm G Dunlop, Susan M Farrington, et al.Familial Cancer|June 14, 2005
Informing one's family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory studyIlse Mesters, Marlein Ausems, Sophie Eichhorn, et al.Familial Cancer|June 14, 2005
SISE matters: the sum of information on seventy-yr-old equivalents measures pedigree information content when assessing the risk of HNPCC in a familyR C Green, J R McLaughlin, H B YounghusbandFamilial Cancer|June 14, 2005
The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li-Fraumeni-like kindredsRina Siddiqui, Kenan Onel, Flavia Facio, et al.Familial Cancer|July 4, 2006
Screening behavior in women at increased familial risk for breast cancerYoland C Antill, John Reynolds, Mary Anne Young, et al.Familial Cancer|March 11, 2006
BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high risk familiesOlga M Sinilnikova, Sylvie Mazoyer, Colette Bonnardel, et al.Familial Cancer|May 11, 2005
Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHxO GimmFamilial Cancer|May 11, 2005
Central nervous system manifestations in VHL: genetics, pathology and clinical phenotypic featuresSven GläskerFamilial Cancer|May 11, 2005
Mutations of the SDHB and SDHD genesChristian Pawlu, Birke Bausch, Hartmut P H NeumannFamilial Cancer|May 11, 2005
Paragangliomas of the head and neck: diagnosis and treatmentC C Boedeker, G J Ridder, J SchipperPageof 151