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Keyword [linkage analysis]
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1. Mapping And Cloning Of Dentinogenesis Imperfecta Type Ⅱ
2. Collecting, Characterizing Of The Genetic Resource And Molecular Mapping Of The Relevant Genes For Hereditary Hearing Impairment
3. Experimental Study On Linkage And Association Between Polymorphisms Within TPO And TSHR Genes And Inherited Thyroid Diseases
4. Preliminary Studies Of Genetic Susceptibility And Susceptible Genes Of Nasopharyngeal Carcinoma
5. Mapping The Disease Gene In A Disseminated Superficial Actinic Porokeratosis Family And Study Susceptibility Genes Of Late-onset Type 2 Diabetes Mellitus
6. Mapping Of Pathogenic Gene In Three DGI-Ⅱ Families
7. Genome-wide Scan Of Graves' Disease In Chinese Han Pedigrees And Epidemiological Study In Pedigrees
8. Asthmatic Epidemiological Study Of Han Nationality In ChongQing China And Primary Study Of Asthmatic Susceptibility Gene Locatization
9. The Study On Genes Associated With An Amyotrophic Lateral Sclerosis Family
10. The Study Of Pedigree And Initial Gene Location For Pathological Myopia
11. Gene Mapping And Mutation Detection In Families With Hereditary Spastic Paraplegia
12. Genome-wide Linkage Analysis And GeneChip～(?) Technology For Susceptibility Genes Contributing To Diabetic Nephropathy In KK/Ta Mice
13. Genetic Research Of Disease-related Mutations And Clinical Study On Periodic Paralyses
14. Identification The Loci For Porokeratosis Palmaris Plantaris Et Disseminata And Disseminated Superficial Porokeratosis And Cloning The Gene Of Disseminated Superficial Porokeratosis
15. Linkage Mapping Of The Two Chinese Family With Autosomal Dominant Retinitis Pigmentosa
16. Genetic Heterogeneity And Gene Diagnosis Of Autosomal Dominant Polycystic Kidney Disease Using Microsatellite DNA And Single Nucleotide Polymorphisms
17. Mapping The Locus For Congenital Preauricular Fistula And A Study Of The Candidate Gene To Schizophrenia
18. Genetic Mapping And Mutation Analysis In Chinese Families With Congenitial Cataract
19. The Phasic Studies On New Susceptible Gene Locus Of Myotonic Dystrophy And Exploration Of The Relationship Of A Brain Specific Gene Seizure-related (SEZ)-6 With Epilepsy
20. Congenital Fibrosis Of The Extraocular Muscles In Chinese Families: Clinical Phenotype, Linkage Mapping, And Mutation Identification Of KIF21A
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