Pages that link to "Q34043662"
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The following pages link to Worldwide genetic analysis of the CFTR region (Q34043662):
Displaying 29 items.
- Initial sequencing and analysis of the human genome (Q21045365) (← links)
- Genetic analysis of African populations: human evolution and complex disease (Q28216772) (← links)
- Linkage disequilibrium in the human genome (Q29616097) (← links)
- Understanding the accuracy of statistical haplotype inference with sequence data of known phase (Q31132499) (← links)
- Testing for homogeneity of gametic disequilibrium across strata (Q33311600) (← links)
- Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD. (Q33488059) (← links)
- Can a place of origin of the main cystic fibrosis mutations be identified? (Q33956009) (← links)
- Gene conversion and different population histories may explain the contrast between polymorphism and linkage disequilibrium levels (Q34020571) (← links)
- Sequence variation and haplotype structure at the human HFE locus (Q34146092) (← links)
- Patterns of linkage disequilibrium in the human genome (Q34609904) (← links)
- Molecular variability in Amerindians: widespread but uneven information (Q34721338) (← links)
- Evolutionary dynamics of the human ABO gene (Q34796574) (← links)
- Signatures of demographic history and natural selection in the human major histocompatibility complex Loci. (Q35038433) (← links)
- Patterns of Human Genetic Diversity: Implications for Human Evolutionary History and Disease (Q35550637) (← links)
- A haplotype framework for cystic fibrosis mutations in Iran (Q35790086) (← links)
- Structure of linkage disequilibrium in humans: genome factors and population stratification (Q35875127) (← links)
- Geographic stratification of linkage disequilibrium: a worldwide population study in a region of chromosome 22. (Q36405335) (← links)
- Effect of single nucleotide polymorphisms on Affymetrix match-mismatch probe pairs (Q36869423) (← links)
- Schistosomal hepatic fibrosis and the interferon gamma receptor: a linkage analysis using single-nucleotide polymorphic markers (Q38911724) (← links)
- Structural analysis of insulin minisatellite alleles reveals unusually large differences in diversity between Africans and non-Africans (Q39487901) (← links)
- Extreme population differences across Neuregulin 1 gene, with implications for association studies. (Q40385572) (← links)
- Haplotype tagging efficiency in worldwide populations in CTLA4 gene (Q40403583) (← links)
- Complete gene scanning by temperature gradient capillary electrophoresis using the cystic fibrosis transmembrane conductance regulator gene as a model (Q41834765) (← links)
- p.F508del in a heterogeneous cystic fibrosis population from Minas Gerais, Brazil (Q46363094) (← links)
- Conservation of the RB1 gene in human and primates (Q46410287) (← links)
- Recombination networks as genetic markers in a human variation study of the Old World (Q46848051) (← links)
- Dynamics of CAG repeat loci revealed by the analysis of their variability (Q46863018) (← links)
- Evaluation of microsatellite markers in association studies: a search for an immune-related susceptibility gene in sarcoidosis. (Q47829526) (← links)
- An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene. (Q52839374) (← links)