A computer programme to calculate risk in X linked disorders using multiple marker loci.

Author:

Clayton J F

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference12 articles.

1. Towards a complete linkage map of the human X chromosome;Wieacker, P.; Davies, K.E.; Cooke, H.J.;Am J Hum Genet,1984

2. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy;Murray, J.M.; Davies, K.E.; Harper, P.S.; Meredith, L.; Mueller, C.R.; Williamson, R.;Nature,1982

3. Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome;Kingston, H.M.; Thomas, N.S.; Pearson, P.L.; Sarfarazi, P.L.; Harper, P.S.;J Med Genet,1983

4. A clinically useful DNA probe closely linked to haemophilia A;Harper, K.; Winter, R.M.; Pembrey, M.E.; Hartley, D.; Davies, K.E.; Tuddenham, E.G.D.;Lancet,1984

5. Close genetic linkage between X linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe LI1.28;Bhattacharya, S.S.; Wright, A.F.; Clayton, J.F.;Nature,1984

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