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Nature Genetics|March 1, 1993
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophyJ Wells, J Wroblewski, J Keen, et al.Nature Genetics|March 1, 1993
Production of a model for Lesch-Nyhan syndrome in hypoxanthine phosphoribosyltransferase-deficient miceC L Wu, D W MeltonNature Genetics|March 1, 1993
A de novo pathological point mutation at the 21-hydroxylase locus: implications for gene conversion in the human genomeS Collier, M Tassabehji, P Sinnott, et al.Nature Genetics|May 3, 2011
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and miceK Saidas Nair, Mounira Hmani-Aifa, Zain Ali, et al.Nature Genetics|May 3, 2011
General properties of transcriptional time series in Escherichia coliLok-Hang So, Anandamohan Ghosh, Chenghang Zong, et al.Nature Genetics|February 1, 1997
Promoter swapping between the genes for a novel zinc finger protein and beta-catenin in pleiomorphic adenomas with t(3;8)(p21;q12) translocationsK Kas, M L Voz, E Röijer, et al.Nature Genetics|February 1, 1997
Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindnessS Yamamoto, K C Sippel, E L Berson, et al.Nature Genetics|February 1, 1997
Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangementsM P Lee, R J Hu, L A Johnson, et al.Nature Genetics|February 1, 1997
Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout miceM Bonyadi, S A Rusholme, F M Cousins, et al.Pageof 742