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Keyword [family-based association]
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1. Establishment Of Haplotype Pattern In The RDH8 And HGF Genes, And The Family-based Association Study With Highmyopia
2. Family-based Association Study Between Human Stat4 Genes Single Nucleotide Polymorphism With Sle In Chinese Han Population
3. Linkage And Association Studies Of Restless Legs Syndrome
4. Association Study Of SNPs Of FcγRâ…¢A Gene And Environmental Factors With Systemic Lupus Erythematosus
5. Family-Based Association Studies Of CAPON And Schizophrenia In The Chinese Han Population
6. Family-Based Association Study Of FTSJ1 With Mental Retardation Of The Population In Qinba Mountain Region
7. Family-based Association Study On DIO2 Polymorphism With Mental Retardation In The Population Of QinBa Mountain Area
8. Genetic Susceptibility Analysis In Primary Biliary Cirrhosis: Family-based Association Test
9. Association Study Between FGD1 Gene And Mental Retardation In The Qinba Mountains-family-based Association Analysis
10. Association Study Between TRAPPC9 Gene And Mental Retardation In Qin-Ba Mountain-family-based Association Analysisi
11. The Association Between The Polymorphisms Of PD-1 And Genetic Susceptibility Of Chronic HBV Infection Family
12. Family-based Association Study Between MTNR Gene And PAI-1 Gene 4G/5G Polymorphisms And PCOS In Han Chinese
13. A Family-based Association Study Of The MDGA1Gene Polymorphisms And Schizophrenia
14. Study On MTMR9 And Non-specific Mental Retardation
15. A family-based association study of conduct disorder
16. Family-based association tests and genetic risk scores for survival data
17. Family-based association studies of the genetic determinants of renal sodium handling
18. Evidence for haplotype-based association in SLE at the c-reactive protein locus: Population-based and family-based association studies
19. Assessing and testing for population stratification and its impact on power of family-based association studies in the United States
20. Statistical methods for family-based association studies for complex human diseases: Single-locus and haplotype methods
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