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Nature Genetics|August 1, 1995
Generation and characterization of a delta F508 cystic fibrosis mouse modelW H Colledge, B S Abella, K W Southern, et al.Nature Genetics|March 1, 1995
A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humansK Yoshida, K Furihata, S Takeda, et al.Nature Genetics|March 1, 1995
Keratin 16 and keratin 17 mutations cause pachyonychia congenitaW H McLean, E L Rugg, D P Lunny, et al.Nature Genetics|October 1, 1993
Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant miceE W Alton, P G Middleton, N J Caplen, et al.Nature Genetics|July 1, 1993
GHRH receptor of little mice contains a missense mutation in the extracellular domain that disrupts receptor functionP Godfrey, J O Rahal, W G Beamer, et al.Nature Genetics|July 1, 1993
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1H T Orr, M Y Chung, S Banfi, et al.Nature Genetics|July 1, 1993
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeatC T Ashley, J S Sutcliffe, C B Kunst, et al.Nature Genetics|July 1, 1993
3,400 new expressed sequence tags identify diversity of transcripts in human brainM D Adams, A R Kerlavage, C Fields, et al.Nature Genetics|July 1, 1993
Functional equivalence of human X- and Y-encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndromeM Watanabe, A R Zinn, D C Page, et al.Nature Genetics|July 1, 1993
Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1S Gispert, R Twells, G Orozco, et al.Pageof 742