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Nature Genetics|October 1, 1995
Long-term hepatic adenovirus-mediated gene expression in mice following CTLA4Ig administrationM A Kay, A X Holterman, L Meuse, et al.Nature Genetics|February 1, 1994
Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndromeM L Reed, S E LeffNature Genetics|November 1, 1993
Missing links: Weber-Cockayne keratin mutations implicate the L12 linker domain in effective cytoskeleton functionE L Rugg, S M Morley, F J Smith, et al.Nature Genetics|September 1, 1994
Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosisR G Crystal, N G McElvaney, M A Rosenfeld, et al.Nature Genetics|December 1, 1995
Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutaseY Li, T T Huang, E J Carlson, et al.Nature Genetics|December 1, 1995
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritanceJ R O'Connell, D E WeeksNature Genetics|December 1, 1995
Transforming growth factor-beta 3 is required for secondary palate fusionG Proetzel, S A Pawlowski, M V Wiles, et al.Nature Genetics|December 1, 1995
A mutation in the mucosal keratin K4 is associated with oral white sponge nevusE L Rugg, W H McLean, W E Allison, et al.Nature Genetics|May 1, 1995
Targeted disruption of the mouse factor VIII gene produces a model of haemophilia AL Bi, A M Lawler, S E Antonarakis, et al.Nature Genetics|May 1, 1995
MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation terminationJ A Enriquez, A Chomyn, G AttardiPageof 742