"Founder" effect in different families with haemophilia B mutation
- 17 February 1990
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 335 (8686), 418
- https://doi.org/10.1016/0140-6736(90)90259-8
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- DIRECT CARRIER TESTING IN 14 FAMILIES WITH HAEMOPHILIA BThe Lancet, 1989
- Mutations in the catalytic domain of human coagulation factor IX: Rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behaviorGenomics, 1989
- DETECTION OF POLYMORPHISMS AT CYTOSINE PHOSPHOGUANADINE DINUCLEOTIDES AND DIAGNOSIS OF HAEMOPHILIA B CARRIERSThe Lancet, 1989
- Diagnostic role of an immunoassay-detected polymorphism of factor IX for potential carriers of hemophilia BBlood, 1988
- Genetic defect responsible for the dysfunctional protein: factor IXLong BeachBlood, 1988
- Use of a BamHI polymorphism in the factor IX gene for the determination of hemophilia B carrier statusBlood, 1986