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Nature Genetics|June 1, 1993
Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomasJ M Cheng, J L Hiemstra, S S Schneider, et al.Nature Genetics|October 1, 1993
Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effectsY P Goldberg, B Kremer, S E Andrew, et al.Nature Genetics|October 1, 1993
Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophyA N Mhatre, M A Trifiro, M Kaufman, et al.Nature Genetics|October 1, 1993
Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, L Pentao, et al.Nature Genetics|October 4, 2000
Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophyC Delettre, G Lenaers, J M Griffoin, et al.Nature Genetics|October 4, 2000
Loss of Gcn5l2 leads to increased apoptosis and mesodermal defects during mouse developmentW Xu, D G Edmondson, Y A Evrard, et al.Nature Genetics|October 4, 2000
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardationK Kutsche, H Yntema, A Brandt, et al.Nature Genetics|September 6, 2000
Domain-specific mutations in TGFB1 result in Camurati-Engelmann diseaseA Kinoshita, T Saito, H Tomita, et al.Pageof 744