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Familial Cancer|June 3, 2017
A novel TP53 germline inframe deletion identified in a Spanish series of Li-fraumeni syndrome suspected familiesPatricia Llovet, Francisco J Illana, Lorena Martín-Morales, et al.Familial Cancer|June 3, 2017
RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancersLochlan J Fennell, Mark Clendenning, Diane M McKeone, et al.Familial Cancer|November 27, 2009
Heterogeneous prevalence of recurrent BRCA1 and BRCA2 mutations in Spain according to the geographical area: implications for genetic testingOrland Diez, Sara Gutiérrez-Enríquez, Judith BalmañaFamilial Cancer|December 4, 2009
Serum antibodies against frameshift peptides in microsatellite unstable colorectal cancer patients with Lynch syndromeMiriam Reuschenbach, Matthias Kloor, Monika Morak, et al.Familial Cancer|December 17, 2009
Mismatch repair protein expression and colorectal cancer in Hispanics from Puerto RicoWilfredo E De Jesus-Monge, Carmen Gonzalez-Keelan, Ronghua Zhao, et al.Familial Cancer|December 8, 2009
Evolving perspectives on genetic discrimination in health insurance among health care providersCarin R Huizenga, Katrina Lowstuter, Kimberly C Banks, et al.Familial Cancer|July 9, 2017
The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genesThomas P Slavin, Susan L Neuhausen, Bita Nehoray, et al.Familial Cancer|April 18, 2018
Prevalence of thyroid diseases in familial adenomatous polyposis: a systematic review and meta-analysisJirat Chenbhanich, Amporn Atsawarungruangkit, Sira Korpaisarn, et al.Familial Cancer|June 28, 2018
Low-level parental mosaicism in an apparent de novo case of Peutz-Jeghers syndromeG I Butel-Simoes, A D Spigelman, R J Scott, et al.Familial Cancer|June 30, 2017
Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from NewfoundlandDaniel R Evans, Jane S Green, Michael O WoodsPageof 151