1)gene screen基因筛查
2)genetic screening[医]基因筛查
3)Mutation screening基因突变筛查
英文短句/例句
1.Screening of the Lipoprotein Lipase Gene for Mutations and the Cloning and Expression of the Human Apolipoprotein CⅡ Gene;人LPL基因突变筛查及人ApoCⅡ基因的克隆和表达
2.Clinical Analysis and Gene Mutation Screening of SCN1B and SCN1A in Generalized Epilepsy with Febrile Seizures Plus Families;GEFS+家系的临床分析及SCN1B、SCN1A基因突变筛查
3.Screening Mutation of CFTR Gene in Man with Congennital Bilateral Absence of Vas Deferens;先天性输精管缺如患者CFTR基因突变筛查
4.Mutation Screening and Whole Spectrum Mutation Map Drawing of GJB2 Gene among Non-syndromic Hearing Impairment Patients;非综合征型耳聋患者GJB2基因突变筛查和全频谱突变图谱绘制
5.Screening the mutations of TMIE gene in genetic nonsyndromic Hearing Loss非综合征性聋分子病因学分析——TMIE基因突变筛查报告
6.LDL-R Function Analysis and Screening of Virulence Gene Mutaion of One "Familial Hypercholesterolemia" Patient;一例“家族性高胆固醇血症”患者LDL-R功能及致病基因突变筛查
7.The Clinical Analysis and Gene Mutation Scree of CLCN1 by PCR-SSCP in Myotonia Congenital Family;先天性肌强直家系的临床分析及CLCN1的基因突变筛查
8.Candidate Gene Screening for Autosomal Dominant Auditory Neuropathy in a Chinese Pedigree;常染色体显性遗传性听神经病家系候选基因突变筛查
9.Detection of ERG11 Mutations in Fluconazole-resistant Candida Albicans Isolates and Application of DNA Array in Identification;耐氟康唑白念珠菌ERG11基因突变筛查及鉴定芯片的研制
10.Screeing of the mtDNA 1555 Mutation Gene Associated with Aminoglycoside-Induced Hearing Loss;AmAn致聋相关mtDNA1555位突变基因的筛查
11.Screening of CYP21 gene P459H mutation by PCR-ACRSPCR-ACRS方法筛查CYP21基因P459H的突变位点
12.A30P and A53T Mutations of the SNCA Gene in α-synucleinopathiesα-突触核蛋白病SNCA基因A30P和A53T的突变筛查
13.The Location and Mutation Screen of Pathogenic Gene of Hereditary Lamellar Cataract;遗传性板层白内障致病基因的定位与突变筛查
14.Mutation Screening of the KCNQ4 and GJB3 Gene in High Frequencies Hearing Loss Population;高频听力下降人群中KCNQ4和GJB3基因的突变筛查
15.Screen of CYP21 Gene P459H Mutation in Adult Han Ethnic Group by PCR-ACRS;PCR-ACRS法筛查成年汉族人CYP21基因P459H的突变位点
16.Mutation Analysis of the CYP1B1 Gene in Primary Congenital Glaucoma Patients;原发性先天性青光眼CYP1B1基因的突变筛查
17.Molecular Scanning for HNF-1α Mutation in Jiangsu Population of Familial Early-onset Diabetes Pedigrees;江苏地区早发糖尿病家系HNF-1α基因突变的筛查
18.Genetic Detection in Two Families with Hereditary Spastic Paraplegias Disease两个HSP家系的致病基因筛查以及突变鉴定
相关短句/例句
genetic screening[医]基因筛查
3)Mutation screening基因突变筛查
4)deafness gene screening聋病基因筛查
5)Gene selection基因筛选
1.This study established mice model using FN(A)P2001, selected the immunogen and protective antigen, and proved that the hemolysin is the protective antigen and prime nosogenetic substance by sequencing of the amino acids of the protective antigen and gene selection.本项研究建立了坏死梭杆菌FN(A)P2001小鼠感染模型,对坏死梭杆菌免疫原及保护性抗原进行了筛选研究,通过对保护性抗原的氨基酸序列测定和基因筛选研究,结合保护性抗原的生物学试验,确定溶血素是坏死梭杆菌的保护性抗原,是致病的主要物质。
6)Gene screen基因筛选
延伸阅读
儿童智力筛查量表儿童智力筛查量表child intelligence screening test 儿童智力筛查皿表(ehild intelligeneescreening test)一种用于筛选检查智力落后儿童的智力测验，由杭州大学心理系弱智儿童问题研究组，于1 986年编制。该测验由十个分测验组成:(l)图画填充。(2)照管日常生活。(3)实物排列(4)计算。协)图片归类。(6)分辨能力。(7)拼木块。(8)数字背诵。(9)划去图形。(10)理解。通过该测验，可鉴别有无智力落后问题，以及智力缺损程度。 (李考忠撰赵亚忠审)
