Pages that link to "Q48036374"
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The following pages link to DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene (Q48036374):
Displaying 50 items.
- Possible ancestral structure in human populations (Q21145263) (← links)
- The Sequence of the Human Genome (Q22065842) (← links)
- The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data (Q22066141) (← links)
- How many diseases does it take to map a gene with SNPs? (Q22337263) (← links)
- Searching for genetic determinants in the new millennium (Q22337300) (← links)
- The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus (Q24533481) (← links)
- Linkage disequilibrium at the ADH2 and ADH3 loci and risk of alcoholism (Q24540214) (← links)
- Sequence variation at two eosinophil-associated ribonuclease loci in humans (Q24548140) (← links)
- A haplotype map of the human genome (Q24679827) (← links)
- Genetics of rheumatoid arthritis: confronting complexity (Q24805024) (← links)
- The genetics of rheumatoid arthritis and the need for animal models to find and understand the underlying genes (Q24805318) (← links)
- Sequence diversity within the HA-1 gene as detected by melting temperature assay without oligonucleotide probes. (Q24814040) (← links)
- SNP-VISTA: an interactive SNP visualization tool (Q25257332) (← links)
- A New Statistical Method for Haplotype Reconstruction from Population Data (Q27860495) (← links)
- Characterization of single-nucleotide polymorphisms in coding regions of human genes (Q28138557) (← links)
- Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis (Q28138570) (← links)
- Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa (Q28142917) (← links)
- DNA sequence variation in a non-coding region of low recombination on the human X chromosome (Q28143669) (← links)
- Polymorphisms in the genes encoding members of the tristetraprolin family of human tandem CCCH zinc finger proteins (Q28182342) (← links)
- A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms (Q28203288) (← links)
- Excess of rare amino acid polymorphisms in the Toll-like receptor 4 in humans (Q28346446) (← links)
- Contrasting patterns of polymorphisms at the ABO-secretor gene (FUT2) and plasma alpha(1,3)fucosyltransferase gene (FUT6) in human populations (Q28366740) (← links)
- Microarray-based sketches of the HERV transcriptome landscape (Q28727826) (← links)
- Human DNA sequence variation in a 6.6-kb region containing the melanocortin 1 receptor promoter (Q28769038) (← links)
- Detecting ancient admixture in humans using sequence polymorphism data (Q28769088) (← links)
- Worldwide DNA sequence variation in a 10-kilobase noncoding region on human chromosome 22 (Q28776624) (← links)
- "Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits. (Q30334349) (← links)
- Maximum likelihood estimation of recombination rates from population data. (Q30619350) (← links)
- Mining SNPs from EST databases (Q30634765) (← links)
- Using step-wise linear regression to detect "functional" sequence variants: application to simulated data. (Q30670312) (← links)
- Analysis of nucleotide sequence data using mixed model methodology. (Q30670354) (← links)
- Use of molecular variation in the NCBI dbSNP database (Q30829552) (← links)
- Expressed sequence tags for the chicken genome from a normalized 10-day-old white leghorn whole-embryo cDNA library. 3. DNA sequence analysis of genetic variation in commercial chicken populations (Q30832892) (← links)
- Development and characterization of expressed sequence tags for the turkey (Meleagris gallopavo) genome and comparative sequence analysis with other birds (Q30841742) (← links)
- Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data (Q30887013) (← links)
- Genome-wide analysis of single-nucleotide polymorphisms in human expressed sequences (Q30936160) (← links)
- An SNP map of human chromosome 22. (Q30940265) (← links)
- Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene (Q30947195) (← links)
- Random mutagenesis-PCR to introduce alterations into defined DNA sequences for validation of SNP and mutation detection methods (Q32163857) (← links)
- Identification of candidate coding region single nucleotide polymorphisms in 165 human genes using assembled expressed sequence tags (Q33179190) (← links)
- Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations (Q33179741) (← links)
- Sequence variation and linkage disequilibrium in the GABA transporter-1 gene (SLC6A1) in five populations: implications for pharmacogenetic research (Q33302969) (← links)
- Sequence variation in the human transcription factor gene POU5F1 (Q33318579) (← links)
- Algorithms to estimate the lower bounds of recombination with or without recurrent mutations (Q33325611) (← links)
- Mining for single nucleotide polymorphisms in pig genome sequence data (Q33397832) (← links)
- From complex traits to complex alleles (Q33543973) (← links)
- Basic concepts in the study of diseases with complex genetics (Q33544009) (← links)
- Sequence organisation of the class II region of the human MHC. (Q33630677) (← links)
- The essence of SNPs (Q33681170) (← links)
- A simple, bead-based approach for multi-SNP molecular haplotyping (Q33754849) (← links)