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Keyword [mutation detection]
Result: 1 - 20 | Page: 1 of 9
1. Development Of System For Mutation Detection Of Autosomal Dominant Polycystic Kidney Disease PKD1 Gene And Its Application In Hans
2. Mutation Patterns In MMR Genes And Clinical Phenotypes Of HNPCC Families In The Northern Chinese Population
3. Gene Mapping And Mutation Detection In Families With Hereditary Spastic Paraplegia
4. Refined Localization Of Dyschromatosis Symmetri Hereditaria Gene To A 9.4-cM Region At Lq21-q22 And Mutation Detection Of ADAR Gene
5. Refined Mapping Of Smith-Fineman-Myers Syndrome And Exclusion Of GPC3,GPC4,MST4,SMARCA1,GPCR2 And Glud2 As Candidate Genes
6. Identification Of A Novel β Thalassemia Mutation And Development Of A Method For High-throughput Mutation Detection Of β-globin Gene
7. Localization Of The Punctate Palmoplantar Keratodermasis Gene By A Genome-wide Scan And Searching For The Disease Gene In A Large Chinese Family
8. Mapping The Disease Gene In SCA Families And The Frequency Distribution Analysis Of Different Subtypes Of SCA In Hans Of China
9. The Study Of Interaction Of Parkin And OGCP And The Mutation Detection Of OGCP Gene
10. Preparation And Analytical Application Of NIR Fluorescent Nanoparticles And Fabrication Of New-Type Biosensing Interfaces For Piezoelectric Immunosensors
11. 1. Genetic Susceptibility Study Of Outcomes After HBV Infection 2. Pharmacogenomics Study Of Hepatitis B By Interferon α 3. Localization And Mutation Detection For Paroxysmal Kinesigenic Choreoathetosis
12. The Effect Of The Interaction Between Mutant Parkin And OGCP On The Apoptosis Of HEK293 Cells And The Mutation Analysis Of HtrA2/Omi Gene In Patients With Parkinson's Disease
13. Molecular Cloning And Characterization Of Mtsarg1-β Mutation Detection Of Polycystic Kidney Disease Gene 1 (PKD1)
14. Clinical Analysis, Pathologic Study And Gene Mutation Detection Of Patients With Fulminant Wilson Disease
15. Location, Identification And Function Research Of Susceptive Genes For Developmental Dislocation Of The Hip In Chromosome Region 17q21
16. Mutation Detection And Functional Study Of Related Genes Of Enlarged Vestibular Aqueduct Syndrome
17. Genetic Characteristic And Gene Mutation Detection In One Familial Parkinson Disease
18. Mapping And Mutation Detection Of Causative Genes For Idiopathic Epilepsy Syndromes FCTE And BFIS, And Mutation Detection For GEFS+
19. Colon Off The Significance Of The Cells And Their Mutations In Genetic Testing In The Diagnosis Of Colorectal Cancer
20. Bone Marrow Proliferative Diseases And Mast Cell Disease, The Receptor Tyrosine Kinase Gene Mutation Detection And Analysis
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