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Journal Articles

Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells

Marguerite Neerman-Arbez, Myrna Germanos-Haddad, Konstantinos Tzanidakis, Dung Vu, Samuel Deutsch, Armelle David, Michael A. Morris, Philippe de Moerloose

Blood (2004) 104 (12): 3618–3623.

https://doi.org/10.1182/blood-2004-06-2312

Published: 2004

Journal Articles

Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion

Dung Vu, Paula H. B. Bolton-Maggs, Jeremy R. Parr, Michael A. Morris, Philippe de Moerloose, Marguerite Neerman-Arbez

Blood (2003) 102 (13): 4413–4415.

https://doi.org/10.1182/blood-2003-06-2141

Published: 2003

Journal Articles

Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family

Marguerite Neerman-Arbez, Dung Vu, Bassam Abu-Libdeh, Isabelle Bouchardy, Michael A. Morris

Blood (2003) 101 (9): 3492–3494.

https://doi.org/10.1182/blood-2002-10-3116

Published: 2003

Journal Articles

Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G→T

Catia Attanasio, Philippe de Moerloose, Stylianos E. Antonarakis, Michael A. Morris, Marguerite Neerman-Arbez

Blood (2001) 97 (6): 1879–1881.

https://doi.org/10.1182/blood.V97.6.1879

Published: 2001

Journal Articles

Mutations in the fibrinogen Aα gene account for the majority of cases of congenital afibrinogenemia

Marguerite Neerman-Arbez, Philippe de Moerloose, Claire Bridel, Ariane Honsberger, Anni Schönbörner, Colette Rossier, Kathelijne Peerlinck, Ségolène Claeyssens, Donna Di Michele, Roseline d'Oiron, Marie Dreyfus, Monique Laubriat-Bianchin, Jacelyne Dieval, Stylianos E. Antonarakis, Michael A. Morris

Blood (2000) 96 (1): 149–152.

https://doi.org/10.1182/blood.V96.1.149

Published: 2000

NARROW

Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells

Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion

Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family

Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G→T

Mutations in the fibrinogen Aα gene account for the majority of cases of congenital afibrinogenemia

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ASH Publications

American Society of Hematology

Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells

Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion

Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family

Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G→T

Mutations in the fibrinogen Aα gene account for the majority of cases of congenital afibrinogenemia

Email alerts

ASH Publications

American Society of Hematology

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