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Results: 5

Authors: Neerman-Arbez, M de Moerloose, P Honsberger, A Parlier, G Arnuti, B Biron, C Borg, JY Eber, S Meili, E Peter-Salonen, K Ripoll, L Vervel, C d'Oiron, R Staeger, P Antonarakis, SE Morris, MA
Citation: M. Neerman-arbez et al., Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes, HUM GENET, 108(3), 2001, pp. 237-240

Authors: Neerman-Arbez, M de Moerloose, P Bridel, C Honsberger, A Schonborner, A Rossier, C Peerlinck, K Claeyssens, S Di Michele, D d'Oiron, R Dreyfus, M Laubriat-Bianchin, M Dieval, J Antonarakis, SE Morris, MA
Citation: M. Neerman-arbez et al., Mutations in the fibrinogen A alpha gene account for the majority of casesof congenital afibrinogenemia, BLOOD, 96(1), 2000, pp. 149-152

Authors: Neerman-Arbez, M Antonarakis, SE Honsberger, A Morris, MA
Citation: M. Neerman-arbez et al., The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster, EUR J HUM G, 7(8), 1999, pp. 897-902

Authors: Neerman-Arbez, M Honsberger, A Antonarakis, SE Morris, MA
Citation: M. Neerman-arbez et al., Deletion of the fibrinogen alpha-chain gene (FGA) causes congenital afibrogenemia (vol 103, pg 215, 1999), J CLIN INV, 103(5), 1999, pp. 759-759

Authors: Neerman-Arbez, M Honsberger, A Antonarakis, SE Morris, MA
Citation: M. Neerman-arbez et al., Deletion of the fibrogen alpha-chain gene (FGA) causes congenital afibrogenemia, J CLIN INV, 103(2), 1999, pp. 215-218
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