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Nature Genetics|January 13, 1998
Neocentromere activity of structurally acentric mini-chromosomes in DrosophilaB C Williams, T D Murphy, M L Goldberg, et al.Nature Genetics|January 13, 1998
Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndromeJ Kohlhase, A Wischermann, H Reichenbach, et al.Nature Genetics|January 13, 1998
FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndromeS Xiao, S R Nalabolu, J C Aster, et al.Nature Genetics|December 17, 1997
Positional cloning of the APECED geneK Nagamine, P Peterson, H S Scott, et al.Nature Genetics|December 17, 1997
Rapid accumulation of genome rearrangements in liver but not in brain of old miceM E Dollé, H Giese, C L Hopkins, et al.Nature Genetics|December 17, 1997
Urokinase-generated plasmin activates matrix metalloproteinases during aneurysm formationP Carmeliet, L Moons, R Lijnen, et al.Nature Genetics|December 17, 1997
Mutations in PEX1 are the most common cause of peroxisome biogenesis disordersB E Reuber, E Germain-Lee, C S Collins, et al.Nature Genetics|December 17, 1997
ATM and RPA in meiotic chromosome synapsis and recombinationA W Plug, A H Peters, Y Xu, et al.Nature Genetics|December 17, 1997
Partial rescue of the prophase I defects of Atm-deficient mice by p53 and p21 null allelesC Barlow, M Liyanage, P B Moens, et al.Nature Genetics|December 17, 1997
Donor splice-site mutations in WT1 are responsible for Frasier syndromeS Barbaux, P Niaudet, M C Gubler, et al.Pageof 744