beta-thalassemia
英
美
网络 β-地中海贫血; β地中海贫血; 地中海贫血症; 地中海贫血
双语例句
- Dr. Huang and his colleagues tried to modify a gene that causes a blood disorder called beta-thalassemia.
黄军及其同事试图修改导致血液疾病β-地中海贫血的一个基因。 - Haploidentical hematopoietic stem cell transplantation for beta-thalassemia major in children
单倍体造血干细胞移植治疗儿童重型β-地中海贫血 - Prenatal diagnosis of a case at-risk for compound heterozygotes of SEA HPFH deletion and β-thalassemia in a Chinese family. Combined transplantation of bone marrow and umbilical cord blood of same sibling in eight children with beta-thalassemia major
缺失型β-地中海贫血一个家系的产前诊断动员后的同胞骨髓联合脐血混合移植治疗儿童重型β-地中海贫血8例 - Combined transplantation of bone marrow and umbilical cord blood of same sibling in eight children with beta-thalassemia major
动员后的同胞骨髓联合脐血混合移植治疗儿童重型β-地中海贫血8例 - Methods NST was performed for two patients with severe aplastic anemia ( SAA) and one with beta-thalassemia major ( TM).
方法对2例重型再障（SAA）和1例重型β-地中海贫血（TM）患者实施NST。 - Clinical study of ten patients with beta-thalassemia major complicated by immune-mediated hemolytic anemia
10例重型β地中海贫血并发急性免疫性溶血的临床分析 - Additionally, 3 cases of abnormal hemoglobinopathy, 7 cases suspected beta-thalassemia were found in the investigation.
此外，还发现异常血红蛋白病3例（0.08%），疑为β-地中海贫血7例。 - Linkage Disequilibrium of RFLP on Beta-Globin Gene Cluster and Its Significance in Prenatal Diagnosis of Beta-Thalassemia
中国人群β珠蛋白基因簇RFLP连锁不平衡及其在产前诊断中的意义 - 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 - Conclusion: The type of gene mutation in beta-thalassemia carriers accompanied with alpha globin gene deletion were multifarious in Shenzhen area.
结论深圳地区合并α珠蛋白基因缺失的β地中海贫血患儿基因突变类型呈现多样性。 - Late-onset infantile metachromatic leukodystrophy without MRI abnormalities in white matter Study on Genotypes of Children with Beta-Thalassemia Major and Their Immune Abnormalities
无脑白质影像学改变的晚发婴儿型异染性脑白质营养不良重型珠蛋白生成障碍性贫血患儿基因突变及免疫紊乱的特点 - Methods: 32 cases of beta-thalassemia screened by routine methods were determined by using gene chip techniques and spot hybridization.
方法对经筛查初诊的32例β地贫进行基因芯片检测并与斑点杂交法进行比较分析。 - Objective: To observe the clinical charateristics, treatment and prognosis of beta-thalassemia major patients complicated by immune-mediated hemolytic anemia.
目的：探讨重型β地中海贫血（重型β地贫）并发急性免疫性溶血的临床特点、治疗和预后。