聋病基因筛查,deafness gene screening英语短句,例句大全

聋病基因筛查,deafness gene screening
1)deafness gene screening聋病基因筛查
2)gene screen基因筛查
3)genetic screening[医]基因筛查
4)Deafness/etiol聋/病因学
5)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