《AmericanJournalofHumanGenetics》期刊第53页199条数据 

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184.《Announcements》

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185.《This Month in the Journal》

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186.《How Malaria Has Affected the Human Genome and What Human Genetics Can Teach Us about Malaria》

genetics_thesis/040004248322.html

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187.《Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations》

genetics_thesis/040004248323.html

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188.《Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome》

genetics_thesis/040004248324.html

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189.《A Combined Genomewide Linkage Scan of 1,233 Families for Prostate Cancer–Susceptibility Genes Conducted by the International Consortium for Prostate Cancer Genetics》

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190.《Weighting Affected Sib Pairs by Marker Informativity》

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191.《A Mutation in SNAP29, Coding for a SNARE Protein Involved in Intracellular Trafficking, Causes a Novel Neurocutaneous Syndrome Characterized by Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma》

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192.《Identification of Risk and Age-at-Onset Genes on Chromosome 1p in Parkinson Disease》

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193.《Allelic Heterogeneity at the Serotonin Transporter Locus (SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors》

genetics_thesis/040004248329.html

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194.《An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains》

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195.《A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy》

genetics_thesis/040004248331.html

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196.《Dysregulation of Chondrogenesis in Human Cleidocranial Dysplasia》

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197.《A “Fille du Roy” Introduced the T14484C Leber Hereditary Optic Neuropathy Mutation in French Canadians》

genetics_thesis/040004248333.html

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198.《A Genomewide Scan for Intelligence Identifies Quantitative Trait Loci on 2q and 6p》

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199.《Use of the Term “Antley-Bixler Syndrome”: Minimizing Confusion》

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