[Intermediate beta thalassemia of the delta-beta (0)/(delta-beta) (0) genotype. Report of a case].
作者信息
Sáenz G F, Carrillo J M, Mora L, Chaves M, Rojas L G, Jiménez R, Jiménez J, Montero A G
出版信息
Sangre (Barc). 1984;29(4-A):467-72.
PMID:6209815
Abstract
摘要
相似文献
1
[Intermediate beta thalassemia of the delta-beta (0)/(delta-beta) (0) genotype. Report of a case].[δ-β(0)/δ-β(0)基因型中间型β地中海贫血。1例报告]
Sangre (Barc). 1984;29(4-A):467-72.
2
delta beta-Thalassemia and HPFH.δβ地中海贫血和遗传性胎儿血红蛋白持续增多症
Birth Defects Orig Artic Ser. 1982;18(7):65-7.
3
Hemoglobin Bart's disease in an Italian boy. Interaction between alpha-thalassemia and hereditary persistence of fetal hemoglobin.一名意大利男孩患血红蛋白Bart's病。α地中海贫血与胎儿血红蛋白遗传性持续存在之间的相互作用。
N Engl J Med. 1990 Jul 19;323(3):179-82. doi: 10.1056/NEJM199007193230307.
4
Thai (delta beta)0-thalassemia and its interaction with gamma-thalassemia.
Hemoglobin. 1988;12(2):101-14. doi: 10.3109/03630268808998017.
5
Deletion and non deletion hereditary persistence of fetal hemoglobin in Italy.意大利胎儿血红蛋白遗传性持续性的缺失型和非缺失型
Haematologica. 1990 Sep-Oct;75 Suppl 5:26-30.
6
Fetal hemoglobin heterogeneity in Brazilian newborns and beta-thalassemia homozygotes.
Haematologica. 1989 Jul-Aug;74(4):347-50.
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
A tentative systematization of beta-thalassemia syndromes present in Northern Sardinia.
Birth Defects Orig Artic Ser. 1982;18(7):169-76.
9
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