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 TitleAuthors / EditorsDate
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Mutational epidemiology of congenital fibrinogen disorders Casini, Alessandro; Blondon, Marc; Tintillier, Veronique; Goodyer, Matthew; ... Neerman Arbez, Marguerite 2018
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Targeted mutation of zebrafish fga models human congenital afibrinogenemia Fish, Richard; Di Sanza, Corinne; Neerman Arbez, Marguerite 2014
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A novel regulatory element between the human FGA and FGG genes Fish, Richard; Neerman Arbez, Marguerite 2012
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Fibrinogen Gdansk: hypofibrinogenemia associated with a novel missense mutation in FGA (Ser112Pro) Mital, Andrzej; Undas, Anetta; Neerman Arbez, Marguerite; Hellmann, Andrzej 2012
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Developmental expression and organisation of fibrinogen genes in the zebrafish Fish, Richard; Vorjohann, Silja; Bena, Frédérique; Fort, Alexandre; Neerman Arbez, Marguerite 2012
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Mutation of the translation initiation codon in FGA causes congenital afibrinogenemia Tirefort, Yordanka; Alson, Olivat Rakoto; De Moerloose, Philippe; Neerman Arbez, Marguerite 2012
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A liver enhancer in the fibrinogen gene cluster Fort, Alexandre; Fish, Richard; Attanasio, Catia; Dosch, Roland; ... Neerman Arbez, Marguerite 2011
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A novel Asp344Val substitution in the fibrinogen gamma chain (fibrinogen Caen) causes dysfibrinogenemia associated with thrombosis Robert-Ebadi, Helia; Le Querrec, Agnès; De Moerloose, Philippe; Gandon-Laloum, Sylvie; ... Neerman Arbez, Marguerite 2008
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Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G→T Attanasio, Catia; De Moerloose, Philippe; Antonarakis, Stylianos; Morris, Michael Andréw; Neerman Arbez, Marguerite 2001