《AmericanJournalofHumanGenetics》期刊第51页200条数据 

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186.《Attention-Deficit/Hyperactivity Disorder in a Population Isolate: Linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11》

genetics_thesis/040004247920.html

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187.《A Genomewide Search Using an Original Pairwise Sampling Approach for Large Genealogies Identifies a New Locus for Total and Low-Density Lipoprotein Cholesterol in Two Genetically Differentiated Isolates of Sardinia》

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188.《Polymorphisms in the Sclerosteosis/van Buchem Disease Gene (SOST) Region Are Associated with Bone-Mineral Density in Elderly Whites》

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189.《A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States》

genetics_thesis/040004247923.html

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190.《CYP3A Variation and the Evolution of Salt-Sensitivity Variants》

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191.《A Second-Generation Genomic Screen for Multiple Sclerosis》

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192.《Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation》

genetics_thesis/040004247926.html

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193.《Genetic Inheritance of Gene Expression in Human Cell Lines》

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194.《Ignoring Linkage Disequilibrium among Tightly Linked Markers Induces False-Positive Evidence of Linkage for Affected Sib Pair Analysis》

genetics_thesis/040004247928.html

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195.《The Genetic or Mythical Ancestry of Descent Groups: Lessons from the Y Chromosome》

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196.《Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder》

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197.《Contractions of D4Z4 on 4qB Subtelomeres Do Not Cause Facioscapulohumeral Muscular Dystrophy》

genetics_thesis/040004247931.html

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198.《CHEK2 Is a Multiorgan Cancer Susceptibility Gene》

genetics_thesis/040004247932.html

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199.《A Common Mutation Is Associated with a Mild, Potentially Asymptomatic Phenotype in Patients with Isovaleric Acidemia Diagnosed by Newborn Screening》

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200.《A Combined Linkage-Physical Map of the Human Genome》

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