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Nature Genetics|May 10, 2000
Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesisG Clarke, A F Goldberg, D Vidgen, et al.Nature Genetics|May 10, 2000
Heterozygous loss of Six5 in mice is sufficient to cause ocular cataractsP S Sarkar, B Appukuttan, J Han, et al.Nature Genetics|May 10, 2000
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2A Bolino, M Muglia, F L Conforti, et al.Nature Genetics|March 30, 2001
The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting statusC Charlier, K Segers, L Karim, et al.Nature Genetics|March 30, 2001
Mutational and functional analyses reveal that ST7 is a highly conserved tumor-suppressor gene on human chromosome 7q31J C Zenklusen, C J Conti, E D GreenNature Genetics|March 30, 2001
Trinucleotide expansion in haploid germ cells by gap repairI V Kovtun, C T McMurrayNature Genetics|February 15, 2001
DSPP mutation in dentinogenesis imperfecta Shields type IIX Zhang, J Zhao, C Li, et al.Nature Genetics|February 15, 2001
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndromeL Crisponi, M Deiana, A Loi, et al.Nature Genetics|April 28, 2001
SOCS-1, a negative regulator of the JAK/STAT pathway, is silenced by methylation in human hepatocellular carcinoma and shows growth-suppression activityH Yoshikawa, K Matsubara, G S Qian, et al.Nature Genetics|April 28, 2001
First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit geneS Baulac, G Huberfeld, I Gourfinkel-An, et al.Pageof 745