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Molecular Psychiatry|November 1, 2003
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII geneE Bacchelli, F Blasi, M Biondolillo, et al.Molecular Psychiatry|November 20, 2003
Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effectsS K Loo, S E Fisher, C Francks, et al.American Journal of Human Genetics|July 6, 2000
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorderC S Lai, S E Fisher, J A Hurst, et al.Genomics|April 11, 2000
Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemiaN McDonell, J Ramser, F Francis, et al.Genomics|November 5, 1997
A sequence-ready physical map of a region of 12q24.1B Renault, A Hovnanian, S Bryce, et al.Genomics|October 27, 1997
Novel genes mapping to the critical region of the 5q- syndromeJ Boultwood, C Fidler, P Soularue, et al.Nature Genetics|May 10, 2000
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2A Bolino, M Muglia, F L Conforti, et al.Genomics|September 24, 1999
Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3)A H Németh, D Nolte, E Dunne, et al.Human Molecular Genetics|April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pumpR Sudbrak, J Brown, C Dobson-Stone, et al.Genomics|February 16, 2000
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22A Bolino, E R Levy, M Muglia, et al.Pageof 29