Prenatal exclusion of severe factor VII deficiency by DNA sequencing
- 30 May 1992
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 339 (8805) , 1359
- https://doi.org/10.1016/0140-6736(92)92005-z
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Recurrent deletion in the human antithrombin III geneBlood, 1991
- Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected maleBlood, 1991
- A common genetic polymorphism associated with lower coagulation factor VII levels in healthy individuals.Arteriosclerosis and Thrombosis: A Journal of Vascular Biology, 1991
- The human factor VII gene is polymorphic due to variation in repeat copy number in a minisatelliteGene, 1988
- Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation.Proceedings of the National Academy of Sciences, 1987
- Hereditary factor VII deficiency: heterogeneity defined by combined functional and immunochemical analysisBlood, 1985