The Molecular Genetics of Haemophilia A and B
- 1 January 1986
- journal article
- review article
- Published by The Company of Biologists in Journal of Cell Science
- Vol. 1986 (Supplement) , 445-458
- https://doi.org/10.1242/jcs.1986.supplement_4.24
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
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- Hemophilia ANew England Journal of Medicine, 1985
- Haemophilia B caused by a point mutation in a donor splice junction of the human factor IX geneNature, 1985
- Genetic disorders of human haemoglobin as models for analysing gene regulationPhilosophical Transactions of the Royal Society of London. B, Biological Sciences, 1984
- Molecular cloning of a cDNA encoding human antihaemophilic factorNature, 1984
- Expression of active human factor VIII from recombinant DNA clonesNature, 1984
- Characterization of the human factor VIII geneNature, 1984
- Assignment of the haemophilia B (Factor IX) locus to the q26‐qter region of the X chromosomeAnnals of Human Genetics, 1984
- Gene deletions in patients with haemophilia B and anti-factor IX antibodiesNature, 1983
- Genetic counselling in haemophilia by discriminant analysis 1975-1980Journal of Medical Genetics, 1982