sanger sequencing - Globe Thesis

Keyword [sanger sequencing] Result: 21 - 40 \| Page: 2 of 4
21.	Clinical Significance Of HBV RT/S Gene Variations In Hepatocellular Carcinoma
22.	The Primary Study Of DYZ1 Array For Distinguishing Monozygotic Twin Males
23.	The Research Of The Association Between BCR-ABL1 Fusion Gene Mutation And TKIs Resistance Based On Next-generation Sequencing
24.	Genetic Screening Of Mutation For Patients With Non-syndromic Hearing Loss And Pathogenic Site Analysis In The Deafness Family With Usher Syndrome
25.	The First Part Of The ZP4 Gene Single Nucleotide Polymorphism And The Chinese Han Population With Primary Open Angle Glaucoma. The Second Part Of A Genetic Stress Susceptibility Peripheral Neuropathy Family Candidate Gene PMP22 Screening Study
26.	A Study Of Common Deafness Genes Using The Combination SNPscan And Sanger Sequencing In Nonsyndromic Hearing Loss Patients Of Minority In Northwest China And Mutation Analysis Of 9 Uncommon Deafness Genes Using SNPscan
27.	Genetic Study Of Pelvic Organ Prolapse
28.	An Identification Of The Disease-causing Genes Of A Hereditary Ataxia Family
29.	The Polymorphism Of Mitochondrial DNA And Association Between Mitochondrial DNA And Schizophrenia
30.	The Application Of Low Level Gene Variants With Sanger Sequencing Traces Using The Ab1 Peak Reporter Tool Of Quantifying In Infectious Diseases Clinical Drug Resistance
31.	Preliminary Identification Of Causative Gene For Tuberous Sclerosis Complex
32.	Screening And Identification Of Disease-Causing Gene In A Mental Retardation Family
33.	Whole Exome Sequencing Identifying Causative Gene In A Migraine Without Aura Pedigree
34.	Establishment And Validation Of The Pyrosequencing Method For Rhesus Box Of RHD Gene And RHC/c Allele Detection
35.	Identification Of Pathogenic Gene In A Family With Hypohidrotic Ectodermal Dysplasia
36.	Expression And Functions Of Circular RNA MART3 In Hypopharyngeal Squamous Cell Carcinoma
37.	Research On The Pathogenic Genes And Related Pathogenic Mechanisms Of Acrokeratoelastoidosis
38.	Mutation Analysis Of The NF1 Gene In Chinese Patients With Neurofibromatosis Type 1.
39.	Screen Of Genes Associated With Normal Skull Morphology Of Han Adults In Liaoning Province Based On Whole-exome Sequencing
40.	An Improved High Resolution Melting Curve For MTHFR C677T Detection
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