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	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: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: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: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

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