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

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Bibliographic Details
Published in:Blood Vol. 101; pp. 3492 - 3494
Main Authors: Neerman Arbez, Marguerite, Vu, Dung, Abu-Libdeh, Bassam, Bouchardy, Isabelle, Morris, Michael Andréw
Format: Journal Article
Language:English
Japanese
Published: American Society of Hematology 01.05.2003
Subjects:
Abortion, Spontaneous
Afibrinogenemia
Afibrinogenemia/ diagnosis/embryology/genetics
Amino Acid Sequence
Amniocentesis
Arabs
Arabs/ genetics
Codon
Codon, Nonsense
Codon/genetics
Consanguinity
DNA, Complementary
DNA, Complementary/genetics
Female
Fetal Diseases
Fetal Diseases/ diagnosis/genetics
Fibrinogen
Fibrinogen/chemistry/ genetics
Genes, Recessive
Genetic Predisposition to Disease
Hemorrhagic Disorders
Hemorrhagic Disorders/genetics
Humans
Infant, Newborn
info:eu-repo/classification/ddc/616
Male
Molecular Sequence Data
Pedigree
ISSN:0006-4971, 1528-0020
Online Access:Get full text
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Description
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2002-10-3116