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281.
Vreugde, S.* et al.: Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. Nat. Genet. 30, 257-258 (2002)
282.
* et al.: Mutations in the gene encoding ε-sarcoglycan cause myoclonus-dystonia syndrome. Nat. Genet. 29, 66-69 (2001)
283.
Werner, T.: The promoter connection. Nat. Genet. 29, 105-106 (2001)
284.
Hrabě de Angelis, M. et al.: Genome-wide, large-scale production of mutant mice by ENU mutagenesis. Nat. Genet. 25, 444-447 (2000)
285.
ADHR Consortium (Lorenz-Depiereux, B. ; Grabowski, M. ; Meitinger, T. ; Strom, T.M.): Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23. Nat. Genet. 26, 345-358 (2000)
286.
Vervoort, R.* et al.: Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. Nat. Genet. 25, 462-466 (2000)
287.
Wiles, M.V.* et al.: Establishment of a gene-trap sequence tag library to generate mutant mice from embryonic stem cells. Nat. Genet. 24, 13-14 (2000)
288.
Timpl, P.* et al.: Impaired stress response and reduced anxiety in mice lacking a functional corticotropin-releasing hormone receptor 1. Nat. Genet. 19, 162-166 (1998)
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