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 deficiency
1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