review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Richard S. Judson | Q43007052 |
Benjamin A. Salisbury | Q51805858 | ||
P2093 | author name string | Andreas Windemuth | |
Julie Schneider | |||
J Claiborne Stephens | |||
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Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28 | Q57232777 | ||
GENOMICS: Genetic Association by Whole-Genome Analysis? | Q57275025 | ||
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease | Q57606857 | ||
Initial sequencing and analysis of the human genome | Q21045365 | ||
The Sequence of the Human Genome | Q22065842 | ||
Are rare variants responsible for susceptibility to complex diseases? | Q22337172 | ||
Searching for genetic determinants in the new millennium | Q22337300 | ||
HGBASE: a database of SNPs and other variations in and around human genes | Q24515305 | ||
A New Statistical Method for Haplotype Reconstruction from Population Data | Q27860495 | ||
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms | Q28203288 | ||
Accessing genetic variation: genotyping single nucleotide polymorphisms | Q28208864 | ||
Linkage disequilibrium in the human genome | Q29616097 | ||
Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease | Q30625643 | ||
Single nucleotide polymorphism libraries: why and how are we building them? | Q30813196 | ||
The essence of SNPs | Q33681170 | ||
Haplotype variation and linkage disequilibrium in 313 human genes | Q33953585 | ||
Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism | Q34144158 | ||
The predictive power of haplotypes in clinical response | Q34189871 | ||
Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase | Q34386645 | ||
Genetic epidemiology of single-nucleotide polymorphisms. | Q36783218 | ||
Molecular haplotyping of genetic markers 10 kb apart by allele-specific long-range PCR. | Q39718282 | ||
Assessment of the total number of human transcription units. | Q40782013 | ||
Irresistible force meets immovable object: SNP mapping of complex diseases | Q46231813 | ||
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Sequence variation in the human angiotensin converting enzyme | Q47964948 | ||
New goals for the U.S. Human Genome Project: 1998-2003. | Q48014748 | ||
Linguistics. From the mouths (and hands) of babes. | Q50490377 | ||
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. | Q52051237 | ||
Gene index analysis of the human genome estimates approximately 120,000 genes. | Q52077979 | ||
Estimation of myriad haplotype frequencies. | Q52682933 | ||
High-resolution haplotype structure in the human genome | Q56002085 | ||
A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1 | Q56566320 | ||
The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes | Q57155049 | ||
P433 | issue | 3 | |
P304 | page(s) | 379-391 | |
P577 | publication date | 2002-05-01 | |
P1433 | published in | Pharmacogenomics | Q15724625 |
P1476 | title | How many SNPs does a genome-wide haplotype map require? | |
P478 | volume | 3 |
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