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Nature Genetics|February 1, 1997
Retinopathy induced in mice by targeted disruption of the rhodopsin geneM M Humphries, D Rancourt, G J Farrar, et al.Nature Genetics|January 1, 1997
Ethical issues in genetic research: disclosure and informed consentP R Reilly, M F Boshar, S H HoltzmanNature Genetics|January 1, 1997
Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndromeC T Basson, D R Bachinsky, R C Lin, et al.Nature Genetics|January 1, 1997
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndromeT D Howard, W A Paznekas, E D Green, et al.Nature Genetics|January 1, 1997
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channelO Zhuchenko, J Bailey, P Bonnen, et al.Nature Genetics|January 1, 1997
UBE3A/E6-AP mutations cause Angelman syndromeT Kishino, M Lalande, J WagstaffNature Genetics|January 1, 1997
Mutations in SOD1 associated with amyotrophic lateral sclerosis cause novel protein interactionsC B Kunst, E Mezey, M J Brownstein, et al.Nature Genetics|March 1, 1997
Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32W C Nichols, D L Koller, B Slovis, et al.Nature Genetics|March 1, 1997
Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1R G Lafrenière, D L Rochefort, N Chrétien, et al.Nature Genetics|March 1, 1997
A non-epistatic interaction of agouti and extension in the fox, Vulpes vulpesD I Våge, D Lu, H Klungland, et al.Pageof 742