| | Title | Authors / Editors | Date |
|
unige:149358 |
Transcription Events in the Origin of Replication of Plasmid pSC101 |
Manen-Commandeur, Danielle; Izaurralde, Elisa; Churchward, Gordon; Caro, Lucien |
1989 |
|
unige:143390 |
Immunogenotyping with antigen receptor gene probes as a diagnostic tool in childhood acute lymphoblastic leukaemia |
Fey, Martin F.; Tobler, Andreas; Stadelmann, Barbara; Hirt, Andreas; ... Wagner, Hans-Peter |
1990 |
|
unige:137163 |
Determination of human alcohol dehydrogenase and acetaldehyde dehydrogenase genotypes by single strand conformation polymorphism in discontinuous buffer electrophoresis |
Walzer, Claude; Turler, Hans; Balant, Luc; Golaz, Olivier Georges; ... von Wartburg, Jean-Pierre |
1993 |
|
unige:8644 |
Normal phenotype with paternal uniparental isodisomy for chromosome 21 |
Blouin, Jean-Louis; Avramopoulos, D.; Pangalos, C.; Antonarakis, Stylianos |
1993 |
|
unige:36652 |
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 |
|
unige:9251 |
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 |
|
unige:9207 |
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 |
|
unige:9248 |
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 |
|
unige:7281 |
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 |
|
unige:11550 |
An in vivo pathway for disulfide bond isomerization in Escherichia coli |
Rietsch, A.; Belin, Dominique; Martin, N.; Beckwith, J. |
1996 |
|
unige:160765 |
Chorea-Acanthocytosis: genetic linkage to chromosome 9q21 |
Rubio, Justin P.; Danek, Adrian; Stone, Caroline; Chalmers, Richard; ... Monaco, Anthony P. |
1997 |
|
unige:74566 |
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 |
|
unige:41508 |
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 |
|
unige:74254 |
Genotype-phenotype correlations in attenuated adenomatous polyposis coli |
Soravia, Claudio; Berk, T; Madlensky, L; Mitri, A; ... Bapat, B |
1998 |
|
unige:29791 |
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 |
|
unige:7417 |
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 |
|
unige:8800 |
Mutation analyses of North American APS-1 patients |
Heino, M.; Scott, Hamish Steele; Chen, Q.; Peterson, P.; ... Krohn, K. |
1999 |
|
unige:8605 |
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 |
|
unige:7289 |
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 |
|
unige:8979 |
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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