Coexistence of Hb Lepore-Boston-Washington (delta 87Gln-beta-IVS-II-8) with alpha-thalassemia [alpha(-5NT)alpha/alpha alpha].
作者信息
Oner C, Oner R, Balkan H, Gümrük F, Gürgey A
机构信息
Department of Biology, Hacettepe University Faculty of Science, Ankara, Turkey.
出版信息
Hemoglobin. 1998 May;22(3):273-6. doi: 10.3109/03630269809113141.
PMID:9629502
Abstract
摘要
相似文献
1
Coexistence of Hb Lepore-Boston-Washington (delta 87Gln-beta-IVS-II-8) with alpha-thalassemia [alpha(-5NT)alpha/alpha alpha].血红蛋白 Lepore-波士顿-华盛顿型（δ87Gln-β-IVS-II-8）与α地中海贫血[α(-5NT)α/αα]共存。
Hemoglobin. 1998 May;22(3):273-6. doi: 10.3109/03630269809113141.
2
Beta-, delta beta-thalassemia and Hb lepore among Yugoslav, Bulgarian, Turkish and Albanian.南斯拉夫、保加利亚、土耳其和阿尔巴尼亚人群中的β-、δβ-地中海贫血和血红蛋白Lepore
Haematologica. 1990 Sep-Oct;75 Suppl 5:31-41.
3
Polycythaemia and microcytosis arising from the combination of a new high oxygen affinity haemoglobin (Hb luton, alpha 89 His-->Leu) and alpha thalassaemia trait.一种新型高氧亲和力血红蛋白（Hb卢顿，α89位组氨酸→亮氨酸）与α地中海贫血特征相结合引起的红细胞增多症和小红细胞症。
Br J Haematol. 1992 Nov;82(3):621-2. doi: 10.1111/j.1365-2141.1992.tb06478.x.
4
Hb Questembert is due to a base substitution (T-->C) in codon 131 of the alpha 2-globin gene and has an alpha-thalassemia biosynthetic ratio.
Am J Hematol. 1995 Apr;48(4):289-90. doi: 10.1002/ajh.2830480419.
5
Hb Lepore-Baltimore (delta 68Leu-beta 84Thr) and Hb Lepore-Washington-Boston (delta 87Gln-beta IVS-II-8) in central Portugal and Spanish Alta Extremadura.葡萄牙中部和西班牙埃斯特雷马杜拉自治区的Lepore-巴尔的摩血红蛋白（δ68Leu-β84Thr）和Lepore-华盛顿-波士顿血红蛋白（δ87Gln-βIVS-II-8）
Hum Genet. 1997 May;99(5):669-73. doi: 10.1007/s004390050426.
6
Hb Gerland [alpha55(E4)Val-->Ala (alpha2)]: a new neutral alpha chain variant involving the alpha2 gene.血红蛋白杰兰德[α55（E4）缬氨酸→丙氨酸（α2）]：一种涉及α2基因的新型中性α链变体。
Hemoglobin. 2001 Nov;25(4):417-20. doi: 10.1081/hem-100107879.
7
Analysis of mRNA from red cells of patients with thalassemia and hemoglobin variants.地中海贫血和血红蛋白变异患者红细胞mRNA分析。
Hemoglobin. 1997 Sep;21(5):437-67. doi: 10.3109/03630269708993129.
8
Hb H disease in association with the silent beta chain variant Hb Hamilton or alpha 2 beta 2(11)(A8)Val----Ile.血红蛋白H病与沉默型β链变异体血红蛋白汉密尔顿或α2β2(11)(A8)缬氨酸→异亮氨酸相关联。
Hemoglobin. 1992;16(5):403-8. doi: 10.3109/03630269209005692.
9
Alpha- and beta-thalassemia in Thailand.泰国的α和β地中海贫血
Ann N Y Acad Sci. 1998 Jun 30;850:412-4. doi: 10.1111/j.1749-6632.1998.tb10507.x.
10
Hb Prato [alpha31(B12)Arg --> Ser (A2)] and alpha-thalassemia in a Taiwanese.
Hemoglobin. 2003 Feb;27(1):45-7. doi: 10.1081/hem-120018436.
Zotero 插件