Published in Genomics on February 01, 1993
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A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17. Nat Genet (1995) 2.16
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A map of 75 human ribosomal protein genes. Genome Res (1998) 2.15
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Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome. Nat Genet (1994) 2.08
Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Mol Psychiatry (2008) 2.07
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Meta-analysis of genome-wide association studies for personality. Mol Psychiatry (2010) 1.96
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Characterization of short tandem repeats from thirty-one human telomeres. Genome Res (1997) 1.96
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Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13. Am J Hum Genet (1996) 1.89
Progress in high throughput SNP genotyping methods. Pharmacogenomics J (2002) 1.88
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