《AmericanJournalofHumanGenetics》期刊第47页200条数据 

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180.《Cloning of Dimethylglycine Dehydrogenase and a New Human Inborn Error of Metabolism, Dimethylglycine Dehydrogenase Deficiency》

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181.《Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome》

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182.《Neuronal Sodium-Channel α1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus》

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183.《A Novel SCN1A Mutation Associated with Generalized Epilepsy with Febrile Seizures Plus—and Prevalence of Variants in Patients with Epilepsy》

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184.《Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements》

genetics_thesis/040004247118.html

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185.《Melanocortin-1 Receptor Gene Variants Determine the Risk of Nonmelanoma Skin Cancer Independently of Fair Skin and Red Hair》

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186.《Localization of a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, PARK6, on Human Chromosome 1p35-p36》

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187.《Evaluation of Linkage and Association of HPC2/ELAC2 in Patients with Familial or Sporadic Prostate Cancer》

genetics_thesis/040004247121.html

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188.《HPC2 Variants and Screen-Detected Prostate Cancer》

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189.《Whole-Genome Screening in Ankylosing Spondylitis: Evidence of Non-MHC Genetic-Susceptibility Loci》

genetics_thesis/040004247123.html

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190.《A Genomewide Screen in Multiplex Rheumatoid Arthritis Families Suggests Genetic Overlap with Other Autoimmune Diseases》

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191.《Multipoint Linkage-Disequilibrium–Mapping Approach Based on the Case-Parent Trio Design》

genetics_thesis/040004247125.html

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192.《Assessment of Parent-of-Origin Effects in Linkage Analysis of Quantitative Traits》

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193.《Efficient Multipoint Linkage Analysis through Reduction of Inheritance Space》

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194.《A New Statistical Method for Haplotype Reconstruction from Population Data》

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195.《An Extensive Analysis of Y-Chromosomal Microsatellite Haplotypes in Globally Dispersed Human Populations》

genetics_thesis/040004247129.html

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196.《High-Resolution Analysis of Human Y-Chromosome Variation Shows a Sharp Discontinuity and Limited Gene Flow between Northwestern Africa and the Iberian Peninsula》

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197.《Axonemal Dynein Intermediate-Chain Gene (DNAI1) Mutations Result in Situs Inversus and Primary Ciliary Dyskinesia (Kartagener Syndrome)》

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198.《A Genetic Factor for Age-Related Cataract: Identification and Characterization of a Novel Galactokinase Variant, “Osaka,” in Asians》

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199.《Limitations of Chromosome Classification by Multicolor Karyotyping》

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200.《Shwachman-Diamond Syndrome with Exocrine Pancreatic Dysfunction and Bone Marrow Failure Maps to the Centromeric Region of Chromosome 7》

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