Read more about the article Association of two DNA polymorphisms in the alpha-globin gene cluster: implications for genetic analysis.
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Association of two DNA polymorphisms in the alpha-globin gene cluster: implications for genetic analysis.

Abstract A new polymorphic BgI II restriction endonuclease site in the alpha-globin gene complex has been found in Cypriot, Sardinian, and Greek populations. In all cases, this polymorphism is linked…

Continue ReadingAssociation of two DNA polymorphisms in the alpha-globin gene cluster: implications for genetic analysis.
Read more about the article Globin gene mapping studies in Sardinian patients homozygous for beta zero Thalassaemia.
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Globin gene mapping studies in Sardinian patients homozygous for beta zero Thalassaemia.

Abstract The genetic factors responsible for the relatively mild clinical phenotypes of some cases of homozygous beta zero thalassaemia (thalassaemia intermedia) in Sardinia have been evaluated. The frequency of deletion…

Continue ReadingGlobin gene mapping studies in Sardinian patients homozygous for beta zero Thalassaemia.
Read more about the article The molecular basis for the clinical diversity of beta thalassaemia in Cypriots.
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The molecular basis for the clinical diversity of beta thalassaemia in Cypriots.

Abstract Much of the clinical variability in the course of homozygous beta thalassaemia in the Cypriot population can be accounted for by the interaction of alpha thalassaemia and by the…

Continue ReadingThe molecular basis for the clinical diversity of beta thalassaemia in Cypriots.
Read more about the article Thalassaemia intermedia in Cyprus: the interaction of alpha and beta thalassaemia.
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Thalassaemia intermedia in Cyprus: the interaction of alpha and beta thalassaemia.

Abstract Restriction endonuclease analysis has been performed on the alpha and beta globin gene clusters of 57 Cypriots homozygous for beta thalassaemia, 30 with the transfusion dependent form of the…

Continue ReadingThalassaemia intermedia in Cyprus: the interaction of alpha and beta thalassaemia.
Read more about the article Hb Summer Hill or alpha 2 beta 2(52)(D3)Asp replaced by His in a Turkish family from Cyprus.
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Hb Summer Hill or alpha 2 beta 2(52)(D3)Asp replaced by His in a Turkish family from Cyprus.

Abstract

Continue ReadingHb Summer Hill or alpha 2 beta 2(52)(D3)Asp replaced by His in a Turkish family from Cyprus.
Read more about the article Alpha-thalassemia in two Mediterranean populations.
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Alpha-thalassemia in two Mediterranean populations.

Abstract We used restriction endonuclease analysis to determine the incidence of alpha-thalassemia in two Mediterranean islands. In a random population sample, the gene frequency of deletion-type alpha-thalassemia-2 (-alpha) was 0.18…

Continue ReadingAlpha-thalassemia in two Mediterranean populations.
Read more about the article Defective vision among Kuwaiti students.
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Defective vision among Kuwaiti students.

Abstract A study, which was intended to find out the main causes of defective vision among Kuwaiti students, yielded the following results: The percentage of defective vision among 139,769 Kuwaiti…

Continue ReadingDefective vision among Kuwaiti students.
Read more about the article Social consequences of introducing antenatal diagnosis for thalassemia.
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Social consequences of introducing antenatal diagnosis for thalassemia.

Abstract

Continue ReadingSocial consequences of introducing antenatal diagnosis for thalassemia.