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A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients Rosatelli, M. C.; Meloni, A.; Devoto, M.; Cao, A.; ... Antonarakis, Stylianos 1998
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A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3 Sertie, A. L.; Quimby, M.; Moreira, E. S.; Murray, J.; ... Passos-Bueno, M. R. 1996
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A linkage disequilibrium map of the MHC region based on the analysis of 14 loci haplotypes in 50 French families Sanchez-Mazas, Alicia; Djoulah, S.; Busson, M.; Le Monnier de Gouville, I.; ... Hors, J. 2000
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A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein Wattenhofer, Marie; Sahin-Calapoglu, Nilufer; Andreasen, Ditte; Kalay, Ersan; ... Antonarakis, Stylianos 2005
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A study of Gm allotypes and immunoglobulin heavy gamma IGHG genes in Berbers, Arabs and sub-Saharan Africans from Jerba Island, Tunisia Loveslati, B Y.; Sanchez-Mazas, Alicia; Ennafaa, H.; Marrakchi, R.; ... Elgaaied, A B. 2001
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A whole-genome association study of major determinants for host control of HIV-1 Fellay, Jacques; Shianna, K. V.; Ge, Dongliang; Colombo, Sara; ... Goldstein, D. B. 2007
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A worldwide population study of the Ag-system haplotypes, a genetic polymorphism of human low-density lipoprotein Breguet, Georges; Bütler, R.; Bütler-Brunner, E.; Sanchez-Mazas, Alicia 1990
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Accurate, scalable and integrative haplotype estimation Delaneau, Olivier; Zagury, Jean-François; Robinson, Matthew R; Marchini, Jonathan L; Dermitzakis, Emmanouil 2019
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Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects Fontana, Pierre; Dupont, Annabelle; Gandrille, Sophie; Bachelot-Loza, Christilla; ... Gaussem, Pascale 2003
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An apportionment of human HLA diversity Sanchez-Mazas, Alicia 2007
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Arg16 homozygosity of the beta2-adrenergic receptor improves the outcome after beta2-agonist tocolysis for preterm labor Landau, Ruth; Morales, M. A.; Antonarakis, Stylianos; Blouin, Jean-Louis; Smiley, R. M. 2005
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Arylamine N-Acetyltransferases in Anthropology Sabbagh, Audrey; Darlu, Pierre; Vangenot, Christelle; Poloni, Estella S. 2018
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Association of a common vitamin D-binding protein polymorphism with inflammatory bowel disease Eloranta, Jyrki J; Wenger, Christa; Mwinyi, Jessica; Hiller, Christian; ... Kullak-Ublick, Gerd A 2011
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Autoimmune T lymphocytes in myasthenia gravis : determination of target epitopes using T lines and recombinant products of the mouse nicotinic acetylcholine receptor gene Melms, A.; Chrestel, S.; Schalke, B.C.; Wekerle, H.; ... Barkas, T. 1989
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Biased allelic expression in human primary fibroblast single cells Borel, Christelle; Ferreira Marinheiro, Pedro; Santoni, Federico; Delaneau, Olivier; ... Antonarakis, Stylianos 2015
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BRD2 and TAP-1 genes and juvenile myoclonic epilepsy Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed 2010
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Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping Kibar, Z.; Dube, M. P.; Powell, J.; McCuaig, C.; ... Rouleau, G. A. 2000
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Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins Scott, Hamish Steele; Heino, M.; Peterson, P.; Mittaz, L.; ... Antonarakis, Stylianos 1998
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Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains Adams, D. J.; Dermitzakis, Emmanouil; Cox, Tony; Smith, James; ... Bradley, Allan 2005
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Control of separate pathogenic autoantibody responses marks MHC gene contributions to murine lupus Vyse, T. J.; Halterman, R. K.; Rozzo, S. J.; Izui, Shozo; Kotzin, B. L. 1999
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