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Nature Genetics|September 1, 1993
Homozygous deletion of the human insulin receptor gene results in leprechaunismE Wertheimer, S P Lu, P F Backeljauw, et al.Nature Genetics|July 1, 1993
Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM geneL A Sabouri, M S Mahadevan, M Narang, et al.Nature Genetics|July 1, 1993
Cloning of human, mouse and fission yeast recombination genes homologous to RAD51 and recAA Shinohara, H Ogawa, Y Matsuda, et al.Nature Genetics|November 1, 1994
PBDX is the XG blood group geneN A Ellis, P Tippett, A Petty, et al.Nature Genetics|June 1, 1995
Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresiaF Vidal, D Aberdam, C Miquel, et al.Nature Genetics|July 1, 1995
Mutation of a type II keratin gene (K6a) in pachyonychia congenitaP E Bowden, J L Haley, A Kansky, et al.Nature Genetics|June 1, 1994
The 1993-94 Généthon human genetic linkage mapG Gyapay, J Morissette, A Vignal, et al.Nature Genetics|November 1, 1995
Linkage between sexual orientation and chromosome Xq28 in males but not in femalesS Hu, A M Pattatucci, C Patterson, et al.Nature Genetics|November 1, 1995
Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient miceK Adlkofer, R Martini, A Aguzzi, et al.Nature Genetics|November 1, 1995
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathiesR Martini, J Zielasek, K V Toyka, et al.Pageof 744