Showing results (241-250 of 316) with videos related to
Sort By:
Pageof 32
Biochemical Genetics|June 1, 1981
Localization of the human fibronectin (FN) gene on chromosome 8 by a specific enzyme immunoassayS I Rennard, R L Church, D H Rohrbach, et al.American Journal of Human Genetics|January 1, 1989
Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markersS D Kittur, M M Bagdon, M L Lubs, et al.American Journal of Medical Genetics|April 15, 2000
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndromeA E Lin, E V Semina, S Daack-Hirsch, et al.Human Mutation|October 23, 2001
Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41Y Watanabe, J C Murray, B C Bjork, et al.The Journal of Biological Chemistry|April 25, 1990
A polypeptide factor produced by fibrosarcoma cells that induces endothelial tissue factor and enhances the procoagulant response to tumor necrosis factor/cachectinM Clauss, J C Murray, M Vianna, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 1, 1997
Clinical and epidemiologic studies of cleft lip and palate in the PhilippinesJ C Murray, S Daack-Hirsch, K H Buetow, et al.American Journal of Human Genetics|April 1, 1987
Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27J C Murray, K H Buetow, M Donovan, et al.Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|September 3, 2015
Prenatal exposure to persistent organic pollutants and offspring allergic sensitization and lung function at 20 years of ageS Hansen, M Strøm, S F Olsen, et al.Journal of Medical Genetics|September 1, 1987
Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genesR E Ferrell, K H Buetow, J K Darby, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1989
Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinomaK H Buetow, J C Murray, J L Israel, et al.Pageof 32