Beta thalassaemia mutations in Turkish Cypriots.

Author:

Sozuoz A,Berkalp A,Figus A,Loi A,Pirastu M,Cao A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference23 articles.

1. Orkin SH, Kazazian HH Jr. The mutation and polymorphism of the human,3-globin genes and its surrounding DNA;Annu Rev Genet,1984

2. Orkin SH, Antonarakis SE, et al.,3-thalassaemia in China: use of in vivo RNA analysis and oligonucleotide hybridization in systematic characterization of molecular defects;Cheng, T.C.;Proc Natl Acad Sci USA,1984

3. Molecular characterization of seven,1-thalassaemia mutations in Asian Indians;Kazazian, H.H.; Orkin, S.H.; Antonarakis, S.E.;EMBO J,1984

4. The molecular basis of,-thalassemia in Lebanon: application to prenatal diagnosis;Chehab, F.F.; Der Kaloustian, V.; Khoori, F.P.; Deeb, S.S.; Kan, Y.W.;Blood,1987

5. A new mutation in IVS-1 of the human,-globin gene causing f3 thalassaemia due to abnormal splicing;Atweh, G.F.; Wong, C.; Reed, R.;Blood,1987

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