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Nature Genetics|September 6, 2000
Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or humanD P Huynh, K Figueroa, N Hoang, et al.Nature Genetics|September 6, 2000
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome ConsortiumM Seri, R Cusano, S Gangarossa, et al.Nature Genetics|May 10, 2000
Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndromeD L Stone, A Slavotinek, G G Bouffard, et al.Nature Genetics|May 10, 2000
Mutations in KERA, encoding keratocan, cause cornea planaN S Pellegata, J L Dieguez-Lucena, T Joensuu, et al.Nature Genetics|May 10, 2000
Dopamine is required for hyperphagia in Lep(ob/ob) miceM S Szczypka, M A Rainey, R D PalmiterNature Genetics|May 10, 2000
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22C Camaschella, A Roetto, A Calì, et al.Nature Genetics|May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusM Satoda, F Zhao, G A Diaz, et al.Nature Genetics|May 10, 2000
Large-scale identification of secreted and membrane-associated gene products using DNA microarraysM Diehn, M B Eisen, D Botstein, et al.Nature Genetics|May 31, 2001
A conserved sorting-associated protein is mutant in chorea-acanthocytosisL Rampoldi, C Dobson-Stone, J P Rubio, et al.Nature Genetics|May 31, 2001
Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubismY Ueki, V Tiziani, C Santanna, et al.Pageof 744