mutation spectrum - Globe Thesis

Keyword [mutation spectrum] Result: 1 - 20 \| Page: 1 of 2
1.	Study Of Human FEN-1 Gene Function And Its Role In The Development Of Genetic Instability
2.	FⅧ Gene Mutation Spectrum In Chinese Hemophilia A Patients
3.	Marfan Syndrome In The Fbn1, Tgfbr2 Genotype Phenotype Association Studies Of Statins On Vascular Endothelial Function Improvement Effect Of Clinical Meta-analysis
4.	Analysis Of Regional Characteristics And Death Cases Of Intrahepatic Cholestasis In Infants Caused By Citrin Defects
5.	Mutation Spectrum And Clinical Features In Infants With Intrahepatic Cholestasis Caused By Citrin Deficiency
6.	Mutation Analysis Of ATP7B Gene In Southern Chinese Wilson Disease Patients By Denaturing High-performance Liquid Chromatography
7.	Mutation Spectrum Of Retnet Genes In Probands With Retinitis Pigmentosa And Associated Diseases
8.	Study On The Protective Effects Of ZiNi Yangyin Shengjin Recipe On Radiation-Injured Mouse HPRT Gene
9.	Mutation Spectrum And Genotype-phenotype Correlation In Chinese OI Patients
10.	The Detection Of Common Mutations In Phenylketonuria And The Mutation Spectrum Of PAH In Chinese Population
11.	Exon Sequencing Analysis Of ATP7B Gene
12.	一、Establishment Of Syndactyly Type Ⅴ Mice Model And Its Morphological Analysis 二、Mutation Spectrum Of Pathogenic Genes In Chinese Patients With Osteogenesis Imperfecta
13.	Analysis Of PAH Gene Mutation Spectrum In Patients With Phenylketonuria In Northwest China And Preliminary Study Of Noninvasive Prenatal Diagnosis
14.	Molecular Diagnosis Of Pediatric Patients With Citrin Deficiency In China:SLC25A13 Mutation Spectrum And The Geographic Distribution
15.	An Analysis On Mutation Spectrum And Promoter Methylation In G6PD Gene
16.	Gene Mutation Spectrum And Prenatal Diagnosis Of Thalassemia In Fujian Region
17.	Molecular Characterization And Gene Mutation Spectrum Of Thalassemia In Fuzhou Area,Fujian Province China
18.	Mutation Spectrum And Phenotypic Manifestation In FSHD Chinese Patients
19.	The Comparative Study Of Esophageal Squamous Cell Carcinoma In Han, Kazak, Uygur, Hui And Mongolian Of China
20.	The Genetic Analysis Of Muscular Dystrophy And Study Of Nevel Mutation
<<First <Prev Next> Last>> Jump to