Prenatal diagnosis of haemophilia B in the first trimester.
Open Access
- 1 October 1987
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 24 (10) , 632
- https://doi.org/10.1136/jmg.24.10.632
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene.Journal of Clinical Investigation, 1984
- CHARACTERISATION AND USE OF AN INTRAGENIC POLYMORPHIC MARKER FOR DETECTION OF CARRIERS OF HAEMOPHILIA B (FACTOR IX DEFICIENCY)The Lancet, 1984