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- 经筛查发现西双版纳州傣族及基诺族G6PD缺乏症的患病率分别为0.2500和0.1395,且后者G6PD缺陷的基因频率为0.1579。The incidence of G6PD deficiency among Dai people is 0.2500 and that among Jinuo people is 0.1395, while the later has a frequency of 0.1579 with defect in the G6PD gene.
- G6PD缺乏症G6PD deficiency
- 目的 建立一种快速、简便的聚合酶链反应(PCR)基因诊断技术检测我国葡萄糖-6-磷酸脱氢酶(G6PD)基因最常见的两种突变型,即G1376T(G6PD Canton)和G1388A(G6PD Kaiping),并初步应用于广西G6PD缺乏症的筛查。Objective: To establish a rapid and simple gene diagnosis technique based on polymerase chain reaction (PCR) for detecting the most two common glucose-6-phosphate dehydrogenase(G6PD)gene mutations in Chinese, namely G1376T (G6PD Canton) and G1388A(G6PD Kaiping) and to apply it for screening the patients with G6PD deficiency in Guangxi.
- G6PD缺乏G6PD; glucose-6-phosphate dehydrogenase deficiency
- 缺乏shortage
- 症obstruction of bowels
- G-CSF治疗白血病化疗不同阶段发生的粒细胞缺乏症疗效观察The observation of the effect of G-CSF on agranulocytosis in different chemotheraphy of acute leukemia
- 铁缺乏症早期early iron-deficiency anemia
- G-6-PD缺乏症G-6-PD deficiency
- 五种微量元素缺乏症防治制剂对肉仔鸡血液甲状腺素水平的影响Effect of the pharmaceutical preparations to prevent and cure trace elements deficiency symptom upon levels of thyroid hormones in blood of chickens
- 四氢生物喋呤缺乏症治疗前后神经系统表现及其脑白质病变分析Clinical manifestations and cerebral white matter changes in children with tetrahydrobiopterin deficiency before and after treatment
- 20-裂解酶缺乏症20-lyase deficiency
- 此外,儿童碘缺乏症造成身体和认知发育障碍以及甲状腺机能减退。In addition, iodine deficiency in children is responsible for disorders in physical and cognitive development, and hypothyroidism.
- 蛋白质缺乏症[营养不良protein malnutrition | kwashiorkor
- 凝血因子Ⅶ缺乏症coagulation factor Ⅶ dificiacy
- 尿苷酸合酶缺乏症deficiency of uridine monophophate synthase
- 四氢生物喋呤缺乏症Tetrahydrob/opterin deficiency
- 微量元素缺乏症(家畜)trace element deficiency, animal
- 多种垂体激素缺乏症muhiple pituitary hormone deficiency