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A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.
Taipale M, Kaminen N, Nopola-Hemmi J, Haltia T, Myllyluoma B, Lyytinen H, Muller K, Kaaranen M, Lindsberg PJ, Hannula-Jouppi K, Kere J. Taipale M, et al. Among authors: kere j. Proc Natl Acad Sci U S A. 2003 Sep 30;100(20):11553-8. doi: 10.1073/pnas.1833911100. Epub 2003 Sep 3. Proc Natl Acad Sci U S A. 2003. PMID: 12954984 Free PMC article.
Global analysis of uniparental disomy using high density genotyping arrays.
Bruce S, Leinonen R, Lindgren CM, Kivinen K, Dahlman-Wright K, Lipsanen-Nyman M, Hannula-Jouppi K, Kere J. Bruce S, et al. Among authors: kere j. J Med Genet. 2005 Nov;42(11):847-51. doi: 10.1136/jmg.2005.032367. Epub 2005 May 6. J Med Genet. 2005. PMID: 15879501 Free PMC article.
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.
Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, Hartung D, Innes M, Kerem B, Nowaczyk MJ, Rivlin J, Roberts W, Senman L, Summers A, Szatmari P, Wong V, Vincent JB, Zeesman S, Osborne LR, Cardy JO, Kere J, Scherer SW, Hannula-Jouppi K. Feuk L, et al. Among authors: kere j. Am J Hum Genet. 2006 Nov;79(5):965-72. doi: 10.1086/508902. Epub 2006 Sep 27. Am J Hum Genet. 2006. PMID: 17033973 Free PMC article.
608 results