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Annals of the Rheumatic Diseases|January 1, 1985
HLA antigens and seronegative rheumatoid arthritisT Bardin, L Legrand, B Naveau, et al.The Journal of Allergy and Clinical Immunology|May 17, 2011
Mold allergen sensitization in adult asthma according to integrin β3 polymorphisms and Toll-like receptor 2/+596 genotypeLidwien A M Smit, Emmanuelle Bouzigon, Jean Bousquet, et al.Plos One|January 5, 2012
A genome-wide association study of the Protein C anticoagulant pathwayGeorgios Athanasiadis, Alfonso Buil, Juan Carlos Souto, et al.Journal of Computer-Aided Molecular Design|December 1, 1994
A shape-based machine learning tool for drug designA N Jain, T G Dietterich, R H Lathrop, et al.Genetics|July 1, 1992
Rat gene mapping using PCR-analyzed microsatellitesT Serikawa, T Kuramoto, P Hilbert, et al.European Journal of Human Genetics : EJHG|June 19, 2008
Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levelsSonia López, Alfonso Buil, Jordi Ordoñez, et al.Contraception|April 17, 2020
Physician and clinic staff attitudes and practices during implementation of the Zika Contraception Access NetworkNaomi K Tepper, Lauren B Zapata, Stacey Hurst, et al.American Journal of Human Genetics|November 1, 1987
Linkage of DNA probe B79a (D7S13) to cystic fibrosisB J Wainwright, L C Tsui, M Leppert, et al.European Journal of Human Genetics : EJHG|June 13, 2013
AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome)Pierre Cacciagli, Jean-Pierre Desvignes, Nadine Girard, et al.European Journal of Human Genetics : EJHG|June 25, 2002
Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutationsMyrna Medlej-Hashim, Mirna Mustapha, Eliane Chouery, et al.Pageof 139