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Nature Genetics|August 1, 1997
Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP geneC A Thornton, J P Wymer, Z Simmons, et al.Nature Genetics|October 1, 1993
Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin geneN Vincent, T Ragot, H Gilgenkrantz, et al.Nature Genetics|October 1, 1993
A novel metalloprotease/disintegrin-like gene at 17q21.3 is somatically rearranged in two primary breast cancersM Emi, T Katagiri, Y Harada, et al.Nature Genetics|October 1, 1993
Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14qJ Hazan, C Lamy, J Melki, et al.Nature Genetics|October 1, 1993
De novo expansion of a (CAG)n repeat in sporadic Huntington's diseaseR H Myers, M E MacDonald, W J Koroshetz, et al.Nature Genetics|October 1, 1993
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2M R Pollak, Y H Chou, J J Cerda, et al.Nature Genetics|June 1, 1997
A functional neo-centromere formed through activation of a latent human centromere and consisting of non-alpha-satellite DNAD du Sart, M R Cancilla, E Earle, et al.Nature Genetics|June 1, 1997
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA geneD Weil, P Küssel, S Blanchard, et al.Nature Genetics|March 9, 2010
Common variants at 5q22 associate with pediatric eosinophilic esophagitisMarc E Rothenberg, Jonathan M Spergel, Joseph D Sherrill, et al.Nature Genetics|March 16, 2010
Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL)Andre Franke, Tobias Balschun, Christian Sina, et al.Pageof 744