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Nature Genetics|January 13, 1998
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newbornsN A Singh, C Charlier, D Stauffer, et al.Nature Genetics|March 1, 1997
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophyR Allikmets, N Singh, H Sun, et al.Genome Biology|June 14, 2013
Comprehensive genotyping of the USA national maize inbred seed bankMaria C Romay, Mark J Millard, Jeffrey C Glaubitz, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007
Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome regionJonathan S Berg, Nicola Brunetti-Pierri, Sarika U Peters, et al.Nature Genetics|January 13, 2009
Increased LIS1 expression affects human and mouse brain developmentWeimin Bi, Tamar Sapir, Oleg A Shchelochkov, et al.Science (New York, N.Y.)|August 8, 2009
The genetic architecture of maize flowering timeEdward S Buckler, James B Holland, Peter J Bradbury, et al.Nature|May 3, 2008
Mapping and sequencing of structural variation from eight human genomesJeffrey M Kidd, Gregory M Cooper, William F Donahue, et al.Pageof 5