Sanger sequencing - Globe Thesis

Keyword [Sanger sequencing] Result: 1 - 20 \| Page: 1 of 4
1.	Detection Of Dengue Virus Using RT-PCR With Tagged Primers In Combination With Sanger Sequencing
2.	Clinical Study On Detection Of Fungi In Paraffin - Embedded Lung Tissues By Molecular Biology
3.	Studies On Mutations Of Deafness Causative Genes In Children Aged0～7Years From Part Of Northwest China
4.	Molecular Diagnosis And Surgical Treatment For Marfan Syndrome
5.	Identification Of Susceptible Genes And Disease-causing Mutations Of Aorta Diseases
6.	Mutation Analysis Of PAH Gene In Patients With PKU And Prenatal Diagnosis In Han Population From Northern China
7.	Mutation Spectrum Of Retnet Genes In Probands With Retinitis Pigmentosa And Associated Diseases
8.	The Relationship Between Phenotype And Genotype For Late-onset Progressive Hearing Loss
9.	Deep Sequencing Identifies Mutation Genes Related To TCCB And Validation Of The HECW1Mutation
10.	Identification Of The Causative Gene Of A Nonsyndromic Retinitis Pigmentosa Pedigree
11.	一、Establishment Of Syndactyly Type Ⅴ Mice Model And Its Morphological Analysis 二、Mutation Spectrum Of Pathogenic Genes In Chinese Patients With Osteogenesis Imperfecta
12.	The Relationship Genotype For Late-onset Progressive Hearing Loss
13.	Explore The Clinical Value Of The HECW1 Gene Mutation And Protein Abnormal Expression In The Diagnosis And Treatment Of Urologic Neoplasms
14.	Several Nucleic Acid Amplification Technologies Research And Their Applications In Mitochondrial DNA Testing
15.	Analysis Of Deafness Genes For Non-syndromic Hearing Loss In Shanxi Province And Prediction Of Function For New Mutations
16.	Cancer Gene Detection And Clinical Application Basing On The Technology Of Ion Torrent Sequencing
17.	Relationship Between EGFR Gene Mutations And Different Phenotypes Of Non-small Cell Lung Cancer
18.	Genetic Analyses Of Polydactyly And Syndactyly
19.	Exome Sequencing Identifies Mutation Genes Related To Intrahepatic Cholangiocarcinoma And Validation Of The USP17 Mutation
20.	Identification Of CDH23 Mutation In A Family With Usher Syndrome
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