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Nature Genetics|August 1, 1993
Rapid cDNA sequencing (expressed sequence tags) from a directionally cloned human infant brain cDNA libraryM D Adams, M B Soares, A R Kerlavage, et al.Nature Genetics|August 1, 1993
Chromosomal distribution of 320 genes from a brain cDNA libraryM H Polymeropoulos, H Xiao, J M Sikela, et al.Nature Genetics|August 1, 1993
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's diseaseR G Snell, J C MacMillan, J P Cheadle, et al.Nature Genetics|August 1, 1993
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's diseaseS E Andrew, Y P Goldberg, B Kremer, et al.Nature Genetics|August 1, 1993
Polygenic control of autoimmune diabetes in nonobese diabetic miceS Ghosh, S M Palmer, N R Rodrigues, et al.Nature Genetics|March 1, 1993
A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 geneC C Hui, A L JoynerNature Genetics|January 24, 2006
Spectrin mutations cause spinocerebellar ataxia type 5Yoshio Ikeda, Katherine A Dick, Marcy R Weatherspoon, et al.Nature Genetics|January 24, 2006
The sex-specific genetic architecture of quantitative traits in humansLauren A Weiss, Lin Pan, Mark Abney, et al.Nature Genetics|January 24, 2006
Evaluating potential for whole-genome studies in Kosrae, an isolated population in MicronesiaPenelope E Bonnen, Itsik Pe'er, Robert M Plenge, et al.Nature Genetics|November 7, 1998
Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient miceL A Pennacchio, D M Bouley, K M Higgins, et al.Pageof 742