Skip to main content

. 1990 Aug 11;18(15):4633. doi: 10.1093/nar/18.15.4633

A less severe form of Haemophilia B Leyden.

M Crossley ¹, P R Winship ¹, D E Austen ¹, C R Rizza ¹, G G Brownlee ¹

PMCID: PMC331323 PMID: 2388855

Abstract

4633

Images in this article

Image
on p.4633

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Briët E., Bertina R. M., van Tilburg N. H., Veltkamp J. J. Hemophilia B Leyden: a sex-linked hereditary disorder that improves after puberty. N Engl J Med. 1982 Apr 1;306(13):788–790. doi: 10.1056/NEJM198204013061306. [DOI] [PubMed] [Google Scholar]
Crossley M., Brownlee G. G. Disruption of a C/EBP binding site in the factor IX promoter is associated with haemophilia B. Nature. 1990 May 31;345(6274):444–446. doi: 10.1038/345444a0. [DOI] [PubMed] [Google Scholar]
Mandalaki T., Louizou C., Dimitriadou C., Briët E. Haemophilia B Leyden in Greece. Thromb Haemost. 1986 Dec 15;56(3):340–342. [PubMed] [Google Scholar]
Reitsma P. H., Bertina R. M., Ploos van Amstel J. K., Riemens A., Briët E. The putative factor IX gene promoter in hemophilia B Leyden. Blood. 1988 Sep;72(3):1074–1076. [PubMed] [Google Scholar]
Reitsma P. H., Mandalaki T., Kasper C. K., Bertina R. M., Briët E. Two novel point mutations correlate with an altered developmental expression of blood coagulation factor IX (hemophilia B Leyden phenotype). Blood. 1989 Feb 15;73(3):743–746. [PubMed] [Google Scholar]
Veltkamp J. J., Meilof J., Remmelts H. G., van der Vlerk D., Loeliger E. A. Another genetic variant of haemophilia B: haemophilia B Leyden. Scand J Haematol. 1970;7(2):82–90. doi: 10.1111/j.1600-0609.1970.tb01873.x. [DOI] [PubMed] [Google Scholar]
Winship P. R. An improved method for directly sequencing PCR amplified material using dimethyl sulphoxide. Nucleic Acids Res. 1989 Feb 11;17(3):1266–1266. doi: 10.1093/nar/17.3.1266. [DOI] [PMC free article] [PubMed] [Google Scholar]

ACTIONS

RESOURCES