β-Thalassemia in four Mediterranean Countries; an Editorial Commentary
- 1 January 1990
- journal article
- editorial
- Published by Taylor & Francis in Hemoglobin
- Vol. 14 (1) , 35-39
- https://doi.org/10.3109/03630269009002253
Abstract
(1990). β-Thalassemia in four Mediterranean Countries; an Editorial Commentary. Hemoglobin: Vol. 14, No. 1, pp. 35-39. doi: 10.3109/03630269009002253Keywords
This publication has 5 references indexed in Scilit:
- A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with “silent” beta-thalassemiaBlood, 1989
- Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probesBlood, 1988
- The molecular basis of beta-thalassemia in Lebanon: application to prenatal diagnosisBlood, 1987
- Sickle cell anaemia among Eti‐Turks: haematological, clinical and genetic observationsBritish Journal of Haematology, 1986
- Hemoglobins Lepore and Anti-LeporeHemoglobin, 1978