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 Incidence of homozygous beta-thalassaemia in New South Wales, 1961-1976.
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Incidence of homozygous beta-thalassaemia in New South Wales, 1961-1976.

Abstract A case-finding survey yielded 58 persons with transfusion-dependent homozygous beta-thalassaemia who lived either in New South Wales or in the Australian Capital Territory. Of those born between 1961 and…

Continue ReadingIncidence of homozygous beta-thalassaemia in New South Wales, 1961-1976.
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.
Read more about the article Haplotypes and levels of fetal hemoglobin and G gamma to A gamma ratios in Mediterranean patients with thalassemia minor and major.
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Haplotypes and levels of fetal hemoglobin and G gamma to A gamma ratios in Mediterranean patients with thalassemia minor and major.

Abstract This study concerned the gamma chain composition of Hb F and the haplotypes of 44 patients with beta-thalassemia major or intermedia and many of their relatives. Seventeen patients came…

Continue ReadingHaplotypes and levels of fetal hemoglobin and G gamma to A gamma ratios in Mediterranean patients with thalassemia minor and major.
Read more about the article Feasibility of prenatal diagnosis of beta-thalassaemia with synthetic DNA probes in two Mediterranean populations.
A rolled newspaper - the left side facing forward. The name of the newspaper is "News" and the words "News" and "Events" are below that. The rubber band keeping the newspaper rolled together is thick and white. There is smaller writing on the newspaper which cannot be read.

Feasibility of prenatal diagnosis of beta-thalassaemia with synthetic DNA probes in two Mediterranean populations.

Abstract A feasibility study in two Mediterranean populations showed that prenatal diagnosis of beta-thalassaemia with a limited number of synthetic oligonucleotide probes would have been possible in about 70% of…

Continue ReadingFeasibility of prenatal diagnosis of beta-thalassaemia with synthetic DNA probes in two Mediterranean populations.
Read more about the article Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat.
A rolled newspaper - the left side facing forward. The name of the newspaper is "News" and the words "News" and "Events" are below that. The rubber band keeping the newspaper rolled together is thick and white. There is smaller writing on the newspaper which cannot be read.

Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat.

Abstract A form of alpha zero-thalassemia found in subjects of Mediterranean origin has been analyzed by gene mapping and DNA sequencing. Homozygotes have the hemoglobin Bart's hydrops fetalis syndrome, while…

Continue ReadingAlpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat.
Read more about the article A new DNA polymorphism for prenatal diagnosis of beta-thalassaemia in Mediterranean populations.
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A new DNA polymorphism for prenatal diagnosis of beta-thalassaemia in Mediterranean populations.

Abstract The prevalence of a new polymorphism for the restriction enzyme Ava II in the psi beta-gene of the beta-globin gene cluster was determined in Mediterranean families with at least…

Continue ReadingA new DNA polymorphism for prenatal diagnosis of beta-thalassaemia in Mediterranean populations.
Read more about the article Feasibility of antenatal diagnosis of beta thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations.
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Feasibility of antenatal diagnosis of beta thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations.

Abstract The feasibility of using restriction fragment length polymorphisms ( RFLPs ) for the antenatal diagnosis of beta thalassaemia in the U.K.-resident Cypriot and Asian Indian populations has been determined.…

Continue ReadingFeasibility of antenatal diagnosis of beta thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations.