AAAAAA
Results:
1-8
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Results: 8
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
Citation: M. Neerman-arbez, The molecular basis of inherited afibrinogenaemia, THROMB HAEM, 86(1), 2001, pp. 154-163
Authors:
Attanasio, C
de Moerloose, P
Antonarakis, SE
Morris, MA
Neerman-Arbez, M
Citation: C. Attanasio et al., Activation of multiple cryptic donor splice sites by the common congenitalafibrinogenemia mutation, FGA IVS4+1 G -> T, BLOOD, 97(6), 2001, pp. 1879-1881
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
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V factor VIII deficiency
Authors:
Neerman-Arbez, M
Johnson, KM
Morris, MA
McVey, JH
Peyvandi, F
Nichols, WC
Ginsburg, D
Rossier, C
Antonarakis, SE
Tuddenham, EGD
Citation: M. Neerman-arbez et al., Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V factor VIII deficiency, BLOOD, 93(7), 1999, pp. 2253-2260
Risultati:
1-8
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