thalassemia发音

意思翻译

n.地中海贫血；库利氏贫血

相似词语短语

thalassemia E───地中海贫血

双语使用场景

Yijie, a 4 year old girl, was diagnosed with thalassemia major when she was just four months old.───王艺洁，一个4岁的女孩，当在4个月大的时候就被诊断出重型地中海贫血病。

using umbilical blood detect the thalassemia to neonate.───应用脐血对新生儿进行地中海贫血的筛查。

Objective To investigate the clinical significance of automated reticulocyte multiple parameters analysis in thalassemia patients.───目的：探讨网织红细胞参数在地中海贫血检测的临床意义。

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。

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。

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。

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。

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。

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。

英语使用场景

Objective To investigate the carrier rate of thalassemia gene in children with decreased mean corpuscular volume(MCV).

Thalassemia is considered a kind of heritable hemolytic disease with high heterology.

Methods: Using man - vessel screen method of thalassemia and relative value of G6PD detect thalassemia and G6PD deficiency for man and woman of detection of before marriage in 4268 duplet .

Mediterranean anemia(thalassemia), occurring relatively often in southern China, is a genetic and hemolytic disease induced by disfunction of globin synthesis.

Methods: Using mon-vessel screen method of thalassemia and relative value of G6PD detect thalassemia and G6PD deficiency for man and woman of detection of before marriage in 4268 duplet.

Objectives To evaluate the early diagnosis way of thalassemia major.

Diseases such as sickle cell anemia and beta thalassemia result from abnormal red blood cells and can be treated with bone-marrow transplants.

A pair of twin girls suffered from thalassemia major.

Free erythrocyte Protoporphyrin(FEP)were determined in 116 thalassemia patients, 37 iron deficiency anemia patients and 45 normal subjects.