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Nature Genetics|December 1, 1992
Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomesB Incerti, S Guioli, A Pragliola, et al.Nature Genetics|December 1, 1992
Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13qK Ben Othmane, M Ben Hamida, M A Pericak-Vance, et al.Nature Genetics|December 1, 1992
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced ageM Corral-Debrinski, T Horton, M T Lott, et al.Nature Genetics|June 1, 1992
The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplicationV Timmerman, E Nelis, W Van Hul, et al.Nature Genetics|June 1, 1992
Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophyC Tsilfidis, A E MacKenzie, G Mettler, et al.Nature Genetics|June 1, 1992
Isolation and characterization of a candidate gene for Norrie diseaseZ Y Chen, R W Hendriks, M A Jobling, et al.Nature Genetics|June 1, 1992
Isolation of chromosome 21-specific yeast artificial chromosomes from a total human genome libraryI M Chumakov, I Le Gall, A Billault, et al.Nature Genetics|September 1, 1992
Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney diseaseR S Kandt, J L Haines, M Smith, et al.Nature Genetics|September 1, 1992
Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4J C Murray, S R Bennett, A E Kwitek, et al.Nature Genetics|September 1, 1992
Genetic dissection of autoimmune type I diabetes in the BB ratH J Jacob, A Pettersson, D Wilson, et al.Pageof 745