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	Title	Authors / Editors	Date
unige:8840	Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A	Lakich, D.; Kazazian, H. H.; Antonarakis, Stylianos; Gitschier, J.	1993
unige:9257	Dinucleotide repeat polymorphism within ERCC5 gene	Samec, S.; Clarkson, S. G.; Blaschak, J.; Chakravarti, A.; ... Antonarakis, Stylianos	1994
unige:9014	TGF-beta 1 influences the relative development of the exocrine and endocrine pancreas in vitro	Sanvito, F.; Herrera, Pedro Luis; Huarte, Joachim; Nichols, A.; ... Vassalli, Jean-Dominique	1994
unige:11311	The large subunit of HIV-1 reverse transcriptase interacts with beta-actin	Hottiger, M.; Gramatikoff, K.; Georgiev, O.; Chaponnier, Christine; ... Hubscher, U.	1995
unige:9217	Characterization of cDNA clones containing CCA trinucleotide repeats derived from human brain	Margolis, R. L.; Breschel, T. S.; Li, S. H.; Kidwai, A. S.; ... Ross, C. A.	1995
unige:9401	Identification of the ligand-binding domain of the surface-located fibrinogen receptor (clumping factor) of Staphylococcus aureus	McDevitt, D.; Francois, Patrice; Vaudaux, Pierre; Foster, T. J.	1995
unige:123120	Use of Amplified Fragment Length Polymorphism in Molecular Typing of Legionella pneumophila and Application to Epidemiological Studies	Valsangiacomo, Claudio; Baggi, Franca; Gaia, Valeria; Balmelli, Tiziano; ... Piffaretti, Jean-Claude	1995
unige:130902	The rat hepatic leukemia factor (HLF) gene encodes two transcriptional activators with distinct circadian rhythms, tissue distributions and target preferences	Falvey, Eileen Elisabeth; Fleury Olela, Fabienne; Schibler, Ulrich	1995
unige:38116	The 5' ends of Hantaan virus (Bunyaviridae) RNAs suggest a prime-and-realign mechanism for the initiation of RNA synthesis	Garcin, Dominique; Lezzi, M; Dobbs, M; Elliott, R M; ... Kolakofsky, Daniel	1995
unige:9142	The 21q22.1 STS marker, VN02 (EST00541 cDNA), is part of the 3' sequence of the human Na+/myo-inositol cotransporter (SLC5A3) gene	Berry, G. T.; Mallee, J. J.; Blouin, Jean-Louis; Antonarakis, Stylianos	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:8843	The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3	Lalioti, M. D.; Gos, A.; Green, M. R.; Rossier, Colette; ... Antonarakis, Stylianos	1996
unige:8648	Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21	Blouin, Jean-Louis; Duriaux Sail, Geneviève; Chen, H.; Gos, A.; ... Antonarakis, Stylianos	1996
unige:9106	The human lanosterol synthase gene maps to chromosome 21q22.3	Young, M.; Chen, H.; Lalioti, M. D.; Antonarakis, Stylianos	1996
unige:8917	YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome	Nadal, M.; Mila, M.; Pritchard, M.; Mur, A.; ... Estivill, X.	1996
unige:84808	Transgenic analysis of a potential Hoxd-11 limb regulatory element present in tetrapods and fish	Beckers, Johannes; Gerard, Matthieu; Duboule, Denis	1996
unige:9027	Isolation of a human gene (HES1) with homology to an Escherichia coli and a zebrafish protein that maps to chromosome 21q22.3	Scott, Hamish Steele; Chen, H.; Rossier, Colette; Lalioti, M. D.; Antonarakis, Stylianos	1997
unige:35088	Dominant-negative suppression of HNF-1alpha function results in defective insulin gene transcription and impaired metabolism-secretion coupling in a pancreatic beta-cell line	Wang, Haiyan; Maechler, Pierre; Hagenfeldt-Johansson, Kerstin Arlette; Wollheim, Claes	1998
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:74595	PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy	Guicheney, P; Vignier, N; Zhang, X; He, Y; ... Tryggvason, K	1998

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