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185.《Ovaries and Female Phenotype in a Girl with 46,XY Karyotype and Mutations in the CBX2 Gene》
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186.《Null Mutations in LTBP2 Cause Primary Congenital Glaucoma》
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187.《Gain-of-Function Mutation of KIT Ligand on Melanin Synthesis Causes Familial Progressive Hyperpigmentation》
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188.《Significant Linkage Evidence for a Predisposition Gene for Pelvic Floor Disorders on Chromosome 9q21》
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189.《Loss of the Metalloprotease ADAM9 Leads to Cone-Rod Dystrophy in Humans and Retinal Degeneration in Mice》
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190.《IFRD1 Is a Candidate Gene for SMNA on Chromosome 7q22-q23》
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191.《Frontorhiny, a Distinctive Presentation of Frontonasal Dysplasia Caused by Recessive Mutations in the ALX3 Homeobox Gene》
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192.《DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III》
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193.《Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations》
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194.《This Month in The Journal》
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195.《This Month in Genetics》
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196.《Revisiting Race in a Genomic Age》
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197.《Association Test for X-Linked QTL in Family-Based Designs》
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198.《Genetic Control of Human Brain Transcript Expression in Alzheimer Disease》
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199.《IFAP Syndrome Is Caused by Deficiency in MBTPS2, an Intramembrane Zinc Metalloprotease Essential for Cholesterol Homeostasis and ER Stress Response》
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200.《Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation》
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