1.
The First Part Association Analysis of the ~G-γ Hemoglobin Gene Promoter -158C/T Polymorphism with Hemoglobin E/β-Thalassemia Major
血红蛋白E/β-地中海贫血~Gγ-珠蛋白基因-158位点的多态性分析
2.
The Study of the Genotypes and Phenotypes Interactions of β-thalassemia/Hemoglobin E in Guangxi Province;
广西地区β-地中海贫血复合异常血红蛋白E的基因型与表现型的研究
3.
Effect of siRNA on the Alpha-Globin of Major Beta-Thalassemia Erythroid Cells Cultured in Vitro;
siRNA对体外培养重型β地中海贫血红系细胞α-珠蛋白的调控作用
4.
Pedigree analysis of the double heterozygote of hemoglobin G disease combined with alpha thalassemia 2
血红蛋白G病复合α地中海贫血2的家系分析
5.
The Best Threshold Value of Hemoglobin A_2 for Diagnosis of β-Thalassemia Carriers by High Performance Liquid Chromatography
高效液相色谱法检测血红蛋白A_2诊断β-地中海贫血携带者的最佳阈值
6.
Analysis of Paramenters of Red Blood Cell in the Screening of β-Thalassaemia Minor
轻型β-地中海贫血的红细胞参数分析
7.
Effects of Liposomal Transfection of Antisense Oligodeoxynucleotide on the Alpha-globin of Major Beta-Thalassemia Erythroid Cells Cultured in Vitro;
脂质体转染反义寡核苷酸对体外培养重型β-地中海贫血红系细胞α-珠蛋白的调控作用
8.
Clinical Value of MCH in Screening Thalassemia
平均血红蛋白量在地中海贫血筛查中的价值探讨
9.
The value of mean corpuscular volume,red cell osmotic fragility test and hemoglobin electrophoresis for prenatal screening of thalassemia
MCV和RBC脆性及血红蛋白电泳在产前筛查地中海贫血的价值
10.
Significance of red blood cell indicators for screening of beta-thalassaemia patients
红细胞参数对β-地中海贫血筛查的意义
11.
PRENATAL DIAGNOSIS OF β-THALASSEMIA--Ⅱ.PRENATAL GENE DIAGNOSIS BY HAPLOTYPING OF THE β-GLOBIN GENE CLUSTER
β-地中海贫血的产前诊断——Ⅰ.用β-珠蛋白基因簇单体型分析进行产前基因诊断
12.
The results were in the normal range. This indicates that these abnormal hemoglobins are rather stable, and the possibility of the Mediterranean anemia is also excluded.
结果均在正常范围,表明这些异常血红蛋白较为稳定,并排除了地中海贫血的可能。
13.
Relationship and Significance of Serum Ferritin,Pretransfusion Mean Hemoglobin and Upgrowth Index in Children with β Thalassemia Major
重型β珠蛋白生成障碍性贫血患儿生长发育指标与血清铁蛋白、血红蛋白量的关系和意义
14.
Beta thalassemia on children: the molecular basis and treatment
儿童β地中海贫血的分子基础和治疗
15.
FTIR-HATR to Identify β-Thalassemia and Its Mechanism Study
FTIR-HATR诊断β-地中海贫血及其机理研究
16.
Molecular Basis of Thalassemia Intermedia
中间型β珠蛋白生成障碍性贫血的分子基础
17.
Investigation of Non-Invasive Prenatal Genetic Diagnosis for B Thalassaemia Using Single Fetal Nucleated Erythrocytes from Maternal Blood;
孕妇外周血中单个胎儿有核红细胞在β地中海贫血无创性产前基因诊断中的应用研究
18.
Analysis of β-thalassemia Mutation in east area of Sichuan
四川东部地区β地中海贫血基因突变分析