Haemophilia A: carrier detection and prenatal diagnosis by linkage analysis using DNA polymorphism.

Author:

Tuddenham E G,Goldman E,McGraw A,Kernoff P B

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference21 articles.

1. Methods for the detection of haemophilia carriers: a memorandum;MA, I.Akhmetali; LM, Aldorf; S, Alexanents;Bull WHO,1977

2. Plasma assay of fetal factor VIIIc and IX for prenatal diagnosis of haemophilia;Mibashan, R.S.; Rodeck, C.H.; Thumpston, J.K.;Lancet,1979

3. DNA analysis in human disease;Wright, A.F.;J Clin Pathol,1986

4. Polymorphic DNA regions adjacent to the 5';Bell, G.I.; Kavam, J.H.; Rutter, W.J.,1981

5. Direct gene analysis of chorionic villi: a possible technique for first-trimester antenatal diagnosis of haemoglobinopathies;Williamson, R.; Eskdale, J.; Coleman, D.V.; Niazi, M.; Loeffler, F.E.; Modell, B.M.;Lancet,1981

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