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Nature Genetics|December 28, 1999
A RA-dependent, tumour-growth suppressive transcription complex is the target of the PML-RARalpha and T18 oncoproteinsS Zhong, L Delva, C Rachez, et al.Nature Genetics|December 28, 1999
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegiaJ Hazan, N Fonknechten, D Mavel, et al.Nature Genetics|October 3, 1999
Structural genomics: beyond the human genome projectS K Burley, S C Almo, J B Bonanno, et al.Nature Genetics|October 3, 1999
Fv2 encodes a truncated form of the Stk receptor tyrosine kinaseD A Persons, R F Paulson, M R Loyd, et al.Nature Genetics|October 3, 1999
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemiaW J Song, M G Sullivan, R D Legare, et al.Nature Genetics|October 3, 1999
Genomic instability in Gadd45a-deficient miceM C Hollander, M S Sheikh, D V Bulavin, et al.Nature Genetics|October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasS Laberge-le Couteulx, H H Jung, P Labauge, et al.Nature Genetics|October 3, 1999
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)A I den Hollander, J B ten Brink, Y J de Kok, et al.Nature Genetics|December 2, 1999
Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosisC Toomes, J James, A J Wood, et al.Nature Genetics|December 2, 1999
Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70J M Warrick, H Y Chan, G L Gray-Board, et al.Pageof 742