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Nature Genetics|January 4, 2001
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin geneK N Alagramam, C L Murcia, H Y Kwon, et al.Nature Genetics|January 4, 2001
Lipodystrophy in the fld mouse results from mutation of a new gene encoding a nuclear protein, lipinM Péterfy, J Phan, P Xu, et al.Nature Genetics|March 10, 2001
DNA double-strand breaks: signaling, repair and the cancer connectionK K Khanna, S P JacksonNature Genetics|March 10, 2001
A temperature-sensitive disorder in basal transcription and DNA repair in humansW Vermeulen, S Rademakers, N G Jaspers, et al.Nature Genetics|March 10, 2001
Chromatin profiling using targeted DNA adenine methyltransferaseB van Steensel, J Delrow, S HenikoffNature Genetics|March 10, 2001
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndromeJ Guy, B Hendrich, M Holmes, et al.Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.Nature Genetics|March 11, 2003
Mutant dynactin in motor neuron diseaseImke Puls, Catherine Jonnakuty, Bernadette H LaMonte, et al.Nature Genetics|March 18, 2003
A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndromeMark O'Driscoll, Victor L Ruiz-Perez, C Geoffrey Woods, et al.Nature Genetics|March 18, 2003
Loss of neuropathy target esterase in mice links organophosphate exposure to hyperactivityChristopher J Winrow, Matthew L Hemming, Duane M Allen, et al.Pageof 744