Heterogeneity of beta/alpha ratio in Italian beta-thalassaemia heterozygotes.
作者信息
Sampietro M, Cappellini M D, Taddei M T, Fiorelli G
出版信息
Haematologica. 1983 Nov-Dec;68(6):703-11.
PMID:6199264
Abstract
摘要
相似文献
1
Heterogeneity of beta/alpha ratio in Italian beta-thalassaemia heterozygotes.意大利β地中海贫血杂合子中β/α比值的异质性。
Haematologica. 1983 Nov-Dec;68(6):703-11.
2
Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levels.血红蛋白A2水平单独升高的纯合子β0地中海贫血杂合子的珠蛋白链合成分析
Nouv Rev Fr Hematol (1978). 1981;23(4):193-5.
3
Thalassemia types in Calabria (Southern Italy).卡拉布里亚（意大利南部）的地中海贫血类型。
Birth Defects Orig Artic Ser. 1982;18(7):147-55.
4
beta-Thalassemia intermedia homozygous for normal hemoglobin A2 beta-thalassemia. Study in four families.中间型β地中海贫血纯合子，伴有正常血红蛋白A2β地中海贫血。对四个家族的研究。
Acta Haematol. 1982;67(1):57-61. doi: 10.1159/000207025.
5
Heterogeneity of beta thalassaemia in Thailand.泰国β地中海贫血的异质性。
Southeast Asian J Trop Med Public Health. 1982 Dec;13(4):618-27.
6
Diagnostic efficacy of haemoglobin A2 in heterozygous beta thalassaemia.血红蛋白A2在杂合子β地中海贫血中的诊断效能
Indian J Med Res. 1984 Aug;80:203-8.
7
Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.正常β-珠蛋白基因的体细胞缺失导致杂合β-地中海贫血患者出现中间型地中海贫血。
Br J Haematol. 2004 Dec;127(5):604-6. doi: 10.1111/j.1365-2141.2004.05237.x.
8
Hematologic changes and hemoglobin analysis beta thalassemia heterozygotes during the first year of life.一岁以内β地中海贫血杂合子的血液学变化及血红蛋白分析
Pediatr Res. 1982 Apr;16(4 Pt 1):286-9. doi: 10.1203/00006450-198204000-00008.
9
[Changes in hemoglobin fractions of pregnant women with heterozygous beta-thalassemia and iron deficiency anemia].[杂合子β地中海贫血合并缺铁性贫血孕妇血红蛋白组分的变化]
Akush Ginekol (Mosk). 1983 Dec(12):41-3.
10
A thalassaemia syndrome resulting from the interaction of delta-beta, beta, and alpha thalassaemia genes. A case report.一种由δ-β、β和α地中海贫血基因相互作用导致的地中海贫血综合征。病例报告。
Pathologica. 1980 Sep-Oct;72(1021):715-21.
Zotero 插件