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High Prevalence of Rare Mutations in the Beta Globin Gene in an Ethnic Group in Iran
High Prevalence Rare Mutations Beta Globin Gene Ethnic Group in Iran
2015/9/23
Beta Thalassemia major is a genetic disease with an autosomal recessive pattern and is differentiated by severe microcytic hypochromic hemolytic anemia with hepatosplenomegaly, ineffective erythropoie...
Abnormal Hemoglobins Associated with Beta-Globin Gene in Antalya Province, Turkey
Abnormal hemoglobins Antalya beta-thalassemia Turkish population
2010/2/24
Some of the abnormal hemoglobin variants found are unstable and some of them cannot be detected by simple electrophoretic examinations. Our findings suggest that abnormal hemoglobins are more frequent...
Effect of the maternal ßE-globin gene on hematologic responses to iron supplementation during pregnancy1,2,3
Hemoglobin E iron supplementation thalassemia serum ferritin pregnancy
2008/12/11
Background: It is customary in Southeast Asia to treat pregnant anemic women with iron supplements, but anemia in this region may be complicated by thalassemia and hemoglobinopathies, which lead to an...
β-Globin Gene Cluster Haplotypes in Iranian Patients with β-Thalassemia
β-globin gene haplotypes thalassemia Iran
2010/4/2
Introduction: β-globin gene cluster haplotypes are useful in diagnosis of particular molecular defects in β-thalassemia, prenatal diagnosis of β-thalassemia, and elucidating population affinities. Met...