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Normal phenotype with paternal uniparental isodisomy for chromosome 21 Blouin, Jean-Louis; Avramopoulos, D.; Pangalos, C.; Antonarakis, Stylianos 1993
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Soluble and cell-bound forms of steel factor activity play distinct roles in melanocyte precursor dispersal and survival on the lateral neural crest migration pathway Wehrle-Haller, Bernhard; Weston, J A 1995
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Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia Rogan, P. K.; Close, P.; Blouin, Jean-Louis; Seip, J. R.; ... Antonarakis, Stylianos 1995
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An in vivo pathway for disulfide bond isomerization in Escherichia coli Rietsch, A.; Belin, Dominique; Martin, N.; Beckwith, J. 1996
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Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus Karayiorgou, M.; Gogos, J. A.; Galke, B. L.; Jeffery, J. A.; ... Pulver, A. E. 1996
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The Johns Hopkins University Collaborative Schizophrenia Study: an epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes Pulver, A. E.; Wolyniec, P. S.; Housman, D.; Kazazian, H. H.; ... Kempf, L. 1996
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A low-fibronectin-binding mutant of Staphylococcus aureus 879R4S has Tn918 inserted into its single fnb gene Greene, C.; Vaudaux, Pierre; Francois, Patrice; Proctor, R. A.; ... Foster, T. J. 1996
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Identification of HLA-DR and -DQ alleles conferring susceptibility to pollen allergy and pollen associated food allergy Boehncke, Wolf-Henning; Loeliger, C.; Kuehnl, P.; Kalbacher, H.; ... Gall, H. 1998
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IgM anti-hepatitis C virus core antibodies as marker of recurrent hepatitis C after liver transplantation Negro, Francesco; Giostra, Emiliano; Rubbia-Brandt, Laura; Mentha, Gilles; ... Hadengue, Antoine 1998
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Genotype-phenotype correlations in attenuated adenomatous polyposis coli Soravia, Claudio; Berk, T; Madlensky, L; Mitri, A; ... Bapat, B 1998
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Different missense mutations in histidine-108 of lysosomal acid lipase cause cholesteryl ester storage disease in unrelated compound heterozygous and hemizygous individuals Ries, S; Büchler, C; Schindler, G; Aslanidis, C; ... Schmitz, G 1998
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Impact of drug resistance mutations on virologic response to salvage therapy. Swiss HIV Cohort Study Lorenzi, P.; Opravil, M.; Hirschel, Bernard; Chave, J. P.; ... Yerly Ferrillo, Sabine 1999
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Randomized, placebo-controlled, double-blind trial to evaluate the efficacy of mupirocin for eradicating carriage of methicillin-resistant Staphylococcus aureus Harbarth, Stéphan Juergen; Dharan, S.; Liassine, N.; Herrault, Pascale; ... Pittet, Didier 1999
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The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations Radhakrishna, U.; Bornholdt, D.; Scott, Hamish Steele; Patel, U. C.; ... Antonarakis, Stylianos 1999
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Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21 Antonarakis, Stylianos; Blouin, Jean-Louis; Lasseter, V. K.; Gehrig, Corinne; ... Pulver, A. E. 1999
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Mutation analyses of North American APS-1 patients Heino, M.; Scott, Hamish Steele; Chen, Q.; Peterson, P.; ... Krohn, K. 1999
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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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Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III Levinson, D. F.; Holmans, P.; Straub, R. E.; Owen, M. J.; ... Mallet, J. 2000
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No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD) Maiti, A. K.; Bartoloni, Lucia; Mitchison, H. M.; Meeks, M.; ... Antonarakis, Stylianos 2000
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Endogenous targets of transcriptional gene silencing in Arabidopsis Steimer, A.; Amedeo, P.; Afsar, K.; Fransz, P.; ... Paszkowski, Jerzy 2000
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