| Title | Authors / Editors | Date |
unige:96873 |
Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy |
Rudolf, Gabrielle; Lesca, Gaetan; Fluss, Joel Victor; Abbas, Mohamed |
2016 |
unige:32871 |
Screening of the THAP1 gene in patients with early-onset dystonia: myoclonic jerks are part of the dystonia 6 phenotype |
Clot, Fabienne; Grabli, David; Burbaud, Pierre; Aya, Magali; ... Brice, Alexis |
2011 |
unige:40095 |
PB1-F2 expression by the 2009 pandemic H1N1 influenza virus has minimal impact on virulence in animal models |
Hai, Rong; Schmolke, Mirco; Varga, Zsuzsanna T; Manicassamy, Balaji; ... Palese, Peter |
2010 |
unige:8595 |
Identification and functional characterization of a novel nonsense mutation in FGA accounting for congenital afibrinogenemia in six Egyptian patients |
Abdel Wahab, Magy; De Moerloose, Philippe; Fish, R. J.; Neerman Arbez, Marguerite |
2010 |
unige:8741 |
Combined factor V - factor VIII deficiency (F5F8D): compound heterozygosity for two novel truncating mutations in LMAN1 in a consanguineous patient |
Farah, R. A.; De Moerloose, Philippe; Bouchardy, Isabelle; Morris, Michael Andréw; ... Neerman Arbez, Marguerite |
2006 |
unige:10198 |
The mental retardation protein PAK3 contributes to synapse formation and plasticity in hippocampus |
Boda, Bernadett; Alberi, Stefano; Nikonenko, Irina; Nodé-Langlois, Roxanne; ... Muller, Dominique |
2004 |
unige:8937 |
Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family |
Neerman Arbez, Marguerite; Vu, Dung; Abu-Libdeh, Bassam; Bouchardy, Isabelle; Morris, Michael Andréw |
2003 |
unige:9079 |
Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion |
Vu, Dung; Bolton-Maggs, P. H.; Parr, J. R.; Morris, Michael Andréw; ... Neerman Arbez, Marguerite |
2003 |
unige:8923 |
The molecular basis of inherited afibrinogenaemia |
Neerman Arbez, Marguerite |
2001 |