1. Application of an intragenic genomic probe to genetic counselling for haemophilia B in the;Connor, J.M.; Pettigrew, A.F.; Hann, I.M.; Forbes, C.D.; Lowe, G.D.O.; Affara, N.A.;west of Scotland. J Med Genet,1985
2. Antenatal diagnosis and carrier detection of haemophilia A using factor VIII gene probe;Gitschier, J.; Lawn, R.M.; Rotblat, F.; Goldman, E.; Tuddenham, E.G.D.;Lancet,1985
3. Gene deletions in patients with haemophilia B and anti-factor IX antibodies;Gianelli, F.; Choo, K.; Rees, D.J.G.;Nature,1983
4. Carrier detection by direct gene analysis in a family with haemophilia B (factor IX deficiency);Peake, I.R.; Furlong, B.L.; Bloom, A.L.;Lancet,1984
5. et aL Gene deletion in an Italian haemophilia B subject;Bernardi, F.; Del Senno, L.; Barbieri, R.;J Med Genet,1985