1. The prenatal diagnosis of 13 thalassaemia;Cao, A.; Pirastu, M.; Rosatelli, C.;Br J Haematol,1986
2. A 13 thalassaemia lesion abolishes the same MstII site as the sickle mutation;Chang, J.C.; Alberti, A.; Kan, Y.W.;Nucleic Acids Res,1983
3. Direct detection of 13039 thalassaemia mutation with MaeI digestion;Weatherall, D.J.; Sampietro, M.; Fiorelli, G.;Lancet,1985
4. Direct detection of the common Mediterranean 13 thalassaemia gene with synthetic DNA probes. An alternative approach for prenatal diagnosis;Orkin, S.H.; Markham, A.F.; Kazazian, H.H.;J Clin Invest,1983
5. Prenatal diagnosis of 1-thalassemia. Detection of a single nucleotide mutation in DNA;Pirastu, M.; Kan, Y.W.; Cao, A.; Conner, B.J.; Teplitz, R.L.; Wallace, R.B.;N Engl J Med,1983