1.地中海贫血症
2.库利氏贫血
1.a hereditary form of anemia, particularly prevalent around the Mediterranean, that is caused by a dysfunction in the synthesis of the red blood pigment hemoglobin
1.A pair of twin girls suffered from thalassemia major.
一对孪生姐妹婴儿患上了重型地中海贫血。
2.Objective To investigate the carrier rate of thalassemia gene in children with decreased mean corpuscular volume(MCV).
目的了解平均红细胞体积（MCV）降低儿童的珠蛋白生成障碍贫血（地贫）基因携带率。
3.Evidence-based recommendations at present rely mainly on the data obtained from intermediate and major thalassemia studies.
当前的循证建议主要依赖中度与重度地中海贫血研究中得出的数据。
4.The thalassemia belt passes through the Mediterranean and West and Central Asian countries.
“地中海贫血症”的分布，则由地中海地区延伸至西亚以及中亚各国。
5.He was also informed that, due to thalassemia gene deletion or mutation is caused by, but not its genetic transmission.
同时他还得知，地中海贫血由于是基因缺失或突变引起的，因此它遗传但不传染。
6.Free erythrocyte Protoporphyrin (FEP)were determined in 116 thalassemia patients, 37 iron deficiency anemia patients and 45 normal subjects.
测定116例珠蛋白生成障碍性贫血、37例缺铁性贫血患者及45例正常人的FEP水平。
7.Experimental study of the red blood cell volume distribution width in iron deficiency anemia and thalassemia
红细胞体积分布宽度在地中海贫血和缺铁性贫血中的实验研究
8.Relationship between the genotype and hematologic characteristics in the fetuses with thalassemia
地中海贫血胎儿产前基因型诊断结果与血象特点的分析
9.The significance of automated reticulocyte multiple parameters analysis in patients with thalassemia
地中海贫血患者网织红细胞多参数分析的意义
10.Thalassemia genotyping and comparison of two diagnostic reagent
地中海贫血的基因诊断及两种试剂比较