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1)  beta-thalassemia/DI
β地中海贫血/诊断
2)  β-thalassemia
β地中海贫血
1.
Study on genic mutation types of β-thalassemia and prenatal diagnosis in Xiamen area;
厦门地区β地中海贫血基因突变类型及产前基因诊断研究
2.
A pilot study on the detection and clinical significance of PRA in children with β-thalassemia major;
重型β地中海贫血患儿群体反应性抗体检测及临床意义
3.
Evaluation of hemoglobin agarose electrophoresis and Hb-F alkali denaturation test in diagnosis of β-Thalassemia;
全自动血红蛋白电泳与Hb-F碱变性试验在β地中海贫血中的应用及评价
3)  Beta-thalassemia
β地中海贫血
1.
Amniotic fluid gene detection in prenatal diagnosis of alpha-and beta-thalassemia;
α和β地中海贫血的羊水产前基因诊断
2.
Closely linked polymorphic marker: successful application in preimplantation genetic diagnosis for beta-thalassemia;
紧密连锁的多态性位点在β地中海贫血植入前遗传学诊断中的应用(英文)
4)  beta thalassemia
β地中海贫血
5)  β thalassemia
β地中海贫血
1.
Identification of a Novel β Thalassemia Mutation and Development of a Method for High-throughput Mutation Detection of β-globin Gene;
β地中海贫血的新突变鉴定和高通量突变检测方法研究
2.
Methods The reverse dot blot technique was employed in the present study for characterization of mutation in 75 fetal umbilical cord blood samples (at least one of parental affected by β thalassemia).
目的 探讨胎儿脐血 Hb A定量在孕中、晚期诊断 β地中海贫血 (β地贫 )的价值。
3.
To investigate the structural and functional stability of an antisencse RNA expression vector in β 654 HeLa cells during the cell subculture,a vector expressing the antisense RNA which targeted against the aberrant splice sites of β thalassemia allele IVS 2 654 C→T(β 654 ) pre mRNA named pCMVA,was constructed in pcDNA3 1.
为研究反义RNA表达载体在细胞内的稳定性,构建了一个特异性针对β地中海贫血基因IVS-2-654C→T(β654)突变mRNA前体异常剪接位点的反义RNA表达载体pCMVA。
6)  β-thalassemia
β-地中海贫血
1.
The Development in β-thalassemia for Gene Therapy;
β-地中海贫血的基因治疗研究
2.
DNA chip construction for β-thalassemia and achondroplasia;
β-地中海贫血与先天性软骨发育不全诊断性基因芯片的构建
3.
Clinical analysis and inquire into interfere measure of 15 cases She nationality children with β-thalassemia in the east of Fujian Province.;
闽东地区畲族小儿β-地中海贫血15例临床分析及干预措施探讨
补充资料:地中海贫血
      一种常染色体显性遗传性疾病,又称海洋性贫血。由于遗传性酶缺陷,血红蛋白A中某个珠蛋白肽链减少或生成受抑制,导致血红蛋白合成障碍而产生贫血。现称珠蛋白生成障碍性贫血。
  
  本病于1925年由T.B.库利等首先描述,虽以地中海区域较多见,但实际遍布世界各民族。中国南方各省,尤其广东、广西也是高发区之一。
  
  临床分为α 和β两大亚型(见珠蛋白生成障碍性贫血)。
  

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