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Nature Genetics|January 4, 2001
A thyroid hormone receptor that is required for the development of green cone photoreceptorsL Ng, J B Hurley, B Dierks, et al.Nature Genetics|January 4, 2001
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1DF Di Palma, R H Holme, E C Bryda, et al.Nature Genetics|January 4, 2001
SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombinationK Myung, A Datta, C Chen, et al.Nature Genetics|January 4, 2001
Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander diseaseM Brenner, A B Johnson, O Boespflug-Tanguy, et al.Nature Genetics|December 28, 1999
A shotgun optical map of the entire Plasmodium falciparum genomeZ Lai, J Jing, C Aston, et al.Nature Genetics|December 28, 1999
Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapsesP D Côté, H Moukhles, M Lindenbaum, et al.Nature Genetics|December 28, 1999
A humanized model for multiple sclerosis using HLA-DR2 and a human T-cell receptorL S Madsen, E C Andersson, L Jansson, et al.Nature Genetics|June 3, 2000
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndromeS Chavanas, C Bodemer, A Rochat, et al.Nature Genetics|June 3, 2000
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedemaM J Karkkainen, R E Ferrell, E C Lawrence, et al.Nature Genetics|June 3, 2000
Features of systemic lupus erythematosus in Dnase1-deficient miceM Napirei, H Karsunky, B Zevnik, et al.Pageof 744