Rapid assessment of haemophilia A carrier state by non-invasive techniques using the polymerase chain reaction.

Author:

Ball J,Warnock L J,Preston F E

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference11 articles.

1. Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragments;Moodie, P.; Liddell, M.B.; Peake, I.R.; Bloom, A.L.;Br J Haematol,1988

2. Genetic mapping and diagnosis of haemophilia A achieved through a Bc1I polymorphism in the factor gene;Gitschier, J.; Drayna, D.; Tuddenham, E.G.D.; White, R.L.; Lawn, R.M.;Nature,1985

3. A new polymorphism in the factor VIII gene for pre-natal diagnosis of haemophilia A;Wion, R.L.; Tuddenham, E.G.D.; Lawn, R.M.;Nucleic Acid Res,1986

4. An improved method for pre-natal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to haemophilia A;Kogan, S.C.; Doherty, A.B.; Gitschier, J.;N Engi J Med,1987

5. Analysis ofhuman Y-chromosomes specific reiterated DNA;Kunkel, L.M.; Smith, K.D.; Boyer, S.H.,1977

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