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Nature Genetics|February 1, 1996
Mutations in the founder of the MIP gene family underlie cataract development in the mouseA Shiels, S BassnettNature Genetics|March 1, 1993
Direct in vivo gene transfer to ependymal cells in the central nervous system using recombinant adenovirus vectorsG Bajocchi, S H Feldman, R G Crystal, et al.Nature Genetics|August 1, 1996
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosisJ N Feder, A Gnirke, W Thomas, et al.Nature Genetics|August 1, 1996
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane proteinJ Kere, A K Srivastava, O Montonen, et al.Nature Genetics|August 1, 1996
A human MSX1 homeodomain missense mutation causes selective tooth agenesisH Vastardis, N Karimbux, S W Guthua, et al.Nature Genetics|August 1, 1996
A common region of 10p deleted in DiGeorge and velocardiofacial syndromesS C Daw, C Taylor, M Kraman, et al.Nature Genetics|August 1, 1996
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21N Rahman, L Arbour, P Tonin, et al.Nature Genetics|August 1, 1996
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics GroupJ L Haines, M Ter-Minassian, A Bazyk, et al.Nature Genetics|August 1, 1996
A full genome search in multiple sclerosisG C Ebers, K Kukay, D E Bulman, et al.Nature Genetics|August 1, 1996
A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2S Kuokkanen, M Sundvall, J D Terwilliger, et al.Pageof 745