1)Enzyme deficiency酶缺陷
英文短句/例句
1.Experimental gene therapy on lipoprotein lipase deficiency脂蛋白脂酶缺陷的实验性基因治疗
2.Laboratory diagnosis of leukocyte myeloperoxidase deficiency白细胞髓过氧化物酶缺陷症的实验诊断
3.Study on Clinical and Pathologic Mechanism of Hereditary Antithrombin Deficiency;遗传性抗凝血酶缺陷症的临床与发病机理研究
4.Kinetic Studies of Erythrocyte Pyruvate Kinase Deficiency;人红细胞丙酮酸激酶缺陷的动力学研究
5.A Clinical Analysis of Glucose-6-Phosphate Dehydrogenase Deficiency in Neonates新生儿葡萄糖-6-磷酸脱氢酶缺陷症的临床分析
6.First Case of Class Ⅰ of Glucose-6-phosphate Dehydrogenase Deficiency in Chinese Population中国人群中首例Ⅰ类葡萄糖-6-磷酸脱氢酶缺陷
7.Right adrenal "tumor-like" hyperplasia in an adult with 21-hydroxylase deficiency-a case report.21-羟化酶缺陷症伴右肾上腺“瘤样”增生1例
8.Diagnosis,treatment and gene mutation analysis in children with holocarboxylase synthetas deficiency羧化全酶合成酶缺陷病的临床诊治及基因突变分析
9.Clinical and molecular genetic analysis for a patient with 17 hydroxylase/17,20 lyase deficiency1例17α-羟化酶/17,20碳链裂解酶缺陷症的临床和分子遗传分析
10.Prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency先天性肾上腺皮质增生症21-羟化酶缺陷的产前诊断一例
11.Frequency of Erythrocyte Pyruvate kinase Deficiency in Cantonese infants广州地区新生儿丙酮酸激酶缺陷基因发生率的研究
12.Functional Complementation of Nitrate Reductase-deficient Mutants in Dunaliella Salina;杜氏盐藻硝酸盐还原酶缺陷型突变株的功能互补分析
13.Study of HGPRT Gene Knock-down and Knock-out Medical Model in Rabbits次黄嘌呤—鸟嘌呤磷酸核糖转移酶缺陷医学模型兔的初步研究
14.Effect of Dipyridamole Therapy on Kawasaki Disease with Glucose-6-Phosphate Dehydrogenase Deficiency in Children双嘧达莫治疗儿童川崎病并葡萄糖-6-磷酸脱氢酶缺陷症的疗效
15.Diagnosis of Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency Using Tandem Mass Spectrometry Combined with in-Vitro Acylcarnitine Profiling Assay成纤维细胞体外培养结合串联质谱酰基肉碱谱诊断极长链酰基辅酶A脱氢酶缺陷症
16.registration fault配准缺陷，重合缺陷
17.Amniotic fluid acetylcholinesterase gel electrophoresis for prenatal diagnosis of neural tube defects羊水乙酰胆碱酯酶凝胶电泳法产前诊断神经管缺陷
18.Construction and in Vitro Metabolic Characterization of Ack Gene Deleted Mutant of Selenomonas Ruminantium反刍月形单胞菌乙酸激酶基因缺陷株的构建及特性分析
相关短句/例句
transketolase deficient转酮酶缺陷
3)Antithrombin deficiency抗凝血酶缺陷症
4)11 beta-hydroxylase deficiency11β-羟化酶缺陷症
1.Clinical characteristics and treatment of 11 beta-hydroxylase deficiency-report of 9 cases and literature review;11β-羟化酶缺陷症9例临床特征与治疗分析
5)21 hydroxylase deficiency21羟化酶缺陷症
1.Objective Clinical data of 19 Chinese patients with 21 hydroxylase deficiency (21OHD) were analyzed to improve the diagnosis and treatment level.目的分析19例21羟化酶缺陷症(21OHD)患者的临床和随访资料,提高该病的诊断和治疗水平。
6)protease-deficient蛋白酶缺陷型
延伸阅读
世间转法转智转无尽【世间转法转智转无尽】 世间转者，谓展转摄前众生界、世界、虚空界也。法转者，谓展转摄前法界、涅槃界、佛出现界也。智转者，谓展转摄前如来智界，心所缘佛智所入境界也。盖此三转，皆言无尽者，以世法智之三种，展转含摄，无有穷尽，是名世间转、法转、智转无尽。
