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Familial Cancer|September 17, 2008
Identification and characterization of a novel MLH1 genomic rearrangement as the cause of HNPCC in a Tunisian family: evidence for a homologous Alu-mediated recombinationSana Aissi-Ben Moussa, Amel Moussa, Tonio Lovecchio, et al.Familial Cancer|October 16, 2008
Prevalence and characteristics of pancreatic cancer in families with BRCA1 and BRCA2 mutationsDaniel H Kim, Beth Crawford, John Ziegler, et al.Familial Cancer|June 14, 2017
Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer familiesMev Dominguez-Valentin, Sigve Nakken, Hélène Tubeuf, et al.Familial Cancer|June 16, 2017
Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomasMark Clendenning, Alvin Huang, Harindra Jayasekara, et al.Familial Cancer|July 19, 2018
Modified capture-recapture estimates of the number of families with Lynch syndrome in Central OhioJohn Michael O Ranola, Rachel Pearlman, Heather Hampel, et al.Familial Cancer|May 29, 2017
Quality of life following prophylactic gynecological surgery: experiences of female Lynch mutation carriersHolly Etchegary, Elizabeth Dicks, Laura Tamutis, et al.Familial Cancer|May 31, 2017
Contiguous gene deletion of chromosome 2p16.3-p21 as a cause of Lynch syndromeErin E Salo-Mullen, Patricio B Lynn, Lu Wang, et al.Familial Cancer|May 22, 2017
Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6Monika Morak, Sarah Käsbauer, Martina Kerscher, et al.Familial Cancer|May 22, 2017
A multi-gene panel study in hereditary breast and ovarian cancer in ColombiaA M Cock-Rada, C A Ossa, H I Garcia, et al.Familial Cancer|June 11, 2017
Co-occurrence of Lynch syndrome and juvenile polyposis syndrome confirmed by multigene panel testingRachel Silva-Smith, Daniel A SussmanPageof 151