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. 1987 Oct;24(10):632. doi: 10.1136/jmg.24.10.632

Prenatal diagnosis of haemophilia B in the first trimester.

Y T Zeng ¹, M L Zhang ¹, Z R Ren ¹, S R Chen ¹, H L Wang ¹, Z Y Wang ¹, J H Tong ¹

PMCID: PMC1050294 PMID: 3681910

632

Selected References

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

Giannelli F., Anson D. S., Choo K. H., Rees D. J., Winship P. R., Ferrari N., Rizza C. R., Brownlee G. G. Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency). Lancet. 1984 Feb 4;1(8371):239–241. doi: 10.1016/s0140-6736(84)90122-3. [DOI] [PubMed] [Google Scholar]
Grunebaum L., Cazenave J. P., Camerino G., Kloepfer C., Mandel J. L., Tolstoshev P., Jaye M., De la Salle H., Lecocq J. P. Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene. J Clin Invest. 1984 May;73(5):1491–1495. doi: 10.1172/JCI111354. [DOI] [PMC free article] [PubMed] [Google Scholar]

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