Prenatal diagnosis of severe factor vii deficiency using mutation detection and linkage analysis
Open Access
- 1 January 2001
- journal article
- research article
- Published by Wiley in British Journal of Haematology
- Vol. 112 (1) , 251-252
- https://doi.org/10.1046/j.1365-2141.2001.02497-4.x
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Exclusion of the First EGF Domain of Factor VII by a Splice Site Mutation Causes Lethal Factor VII DeficiencyBlood, 1998
- Inherited Factor VII Deficiency: Molecular Genetics and PathophysiologyThrombosis and Haemostasis, 1997
- Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7)Human Genetics, 1992
- Prenatal exclusion of severe factor VII deficiency by DNA sequencingThe Lancet, 1992