(Q56002085)

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High-resolution haplotype structure in the human genome

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High-resolution haplotype structure in the human genome (English)

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John D. Rioux

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Eric S. Lander

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Mark Joseph Daly

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Mark J. Daly

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Stephen F Schaffner

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Stephen F. Schaffner

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Thomas J. Hudson

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English

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publication date

October 2001

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229-232

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Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

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Recombinational and mutational hotspots within the human lipoprotein lipase gene

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High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot

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Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

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Linkage disequilibrium and homozygosity of chromosome segments in finite populations

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

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Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes

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Initial sequencing and analysis of the human genome

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Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness

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Identification of new single-nucleotide polymorphisms in the thrombin receptor gene and their effects on coronary artery diseases in Koreans

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Allele associations reveal four prominent haplotypes at the human interleukin-6 (IL-6) locus

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New polymorphisms in the IL-10 promoter region

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Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium

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Single nucleotide polymorphism and linkage disequilibrium within the TCR alpha/delta locus

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Linkage disequilibrium in the human genome

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Haplotype tagging for the identification of common disease genes

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Identifiers

DOI

10.1038/NG1001-229

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PubMed publication ID

11586305

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ResearchGate publication ID

11763944

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