| | Title | Authors / Editors | Date |
|
unige:45205 |
Identification of VPS35 mutations replicated in French families with Parkinson disease |
Lesage, S; Condroyer, C; Klebe, S; Honoré, A; ... Brice, A |
2012 |
|
unige:25139 |
Standardization of DNA isolation from low cell numbers for chimerism analysis by PCR of short tandem repeats |
van der Burg, M; Kreyenberg, H; Willasch, A; Barendregt, B H; ... van Dongen, J J M |
2011 |
|
unige:20742 |
Mild intellectual disability associated with a progeny of father-daughter incest: genetic and environmental considerations |
Ansermet, François; Lespinasse, James; Gimelli, Stefania; Bena, Frédérique; Giacobino, Ariane |
2010 |
|
unige:8803 |
Dominant-negative effects of a novel mutated Ins2 allele causes early-onset diabetes and severe beta-cell loss in Munich Ins2C95S mutant mice |
Herbach, Nadja; Rathkolb, Birgit; Kemter, Elisabeth; Pichl, Lisa; ... Wanke, Ruediger |
2007 |
|
unige:11088 |
Lessons from the bare lymphocyte syndrome: molecular mechanisms regulating MHC class II expression |
Waldburger, Jean-Marc; Masternak, Krzysztof; Muhlethaler-Mottet, Annick; Villard, Jean; ... Reith, Walter |
2000 |
|
unige:11557 |
Enhanced susceptibility to lupus contributed from the nonautoimmune C57BL/10, but not C57BL/6, genome |
Rozzo, S. J.; Vyse, T. J.; Menze, K.; Izui, Shozo; Kotzin, B. L. |
2000 |
|
unige:8930 |
Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia |
Neerman Arbez, Marguerite; De Moerloose, Philippe; Bridel, C.; Honsberger, A.; ... Morris, Michael Andréw |
2000 |
|
unige:9076 |
Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency |
Villard, Jean; Reith, Walter; Barras, Emmanuele; Gos, A.; ... Mach, Bernard |
1997 |
|
unige:10883 |
The A985G mutation in the medium-chain acyl-CoA dehydrogenase gene: high prevalence in the Swiss population resident in Geneva |
Conne, Béatrice; Zufferey, R.; Belin, Dominique |
1995 |
Heterozygote detection
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