{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,29]],"date-time":"2026-01-29T23:33:18Z","timestamp":1769729598405,"version":"3.49.0"},"reference-count":54,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[2005,12,1]],"date-time":"2005-12-01T00:00:00Z","timestamp":1133395200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Ann. of Dyslexia"],"published-print":{"date-parts":[[2005,12]]},"DOI":"10.1007\/s11881-005-0009-4","type":"journal-article","created":{"date-parts":[[2007,7,26]],"date-time":"2007-07-26T07:20:31Z","timestamp":1185434431000},"page":"151-165","source":"Crossref","is-referenced-by-count":38,"title":["Dyslexia\u2014A molecular disorder of neuronal migration"],"prefix":"10.1007","volume":"55","author":[{"given":"Albert M.","family":"Galaburda","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"issue":"3","key":"9_CR1","doi-asserted-by":"crossref","first-page":"607","DOI":"10.1097\/00001756-199902250-00030","volume":"10","author":"M. Best","year":"1999","unstructured":"Best, M., & Demb, J. B. (1999). Normal planum temporale asymmetry in dyslexics with a magnocellular pathway deficit. Neuroreport, 10(3), 607\u2013612.","journal-title":"Neuroreport"},{"issue":"4","key":"9_CR2","doi-asserted-by":"crossref","first-page":"742","DOI":"10.1212\/01.WNL.0000134673.95020.EE","volume":"63","author":"S. M. Brambati","year":"2004","unstructured":"Brambati, S. M., Termine, C., Ruffino, M., Stella, G., Fazio, F., Cappa, S. F., et al. (2004). Regional reductions of gray matter volume in familial dyslexia. Neurology, 63(4), 742\u2013745.","journal-title":"Neurology"},{"key":"9_CR3","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1093\/brain\/123.2.291","volume":"123","author":"L. Cohen","year":"2000","unstructured":"Cohen, L., Dehaene, S., Naccache, L., Lehericy, S., Dehaene-Lambertz, G., Henaff, M. A., et al. (2000). The visual word form area: Spatial and temporal characterization of an initial stage of reading in normal subjects and posterior split-brain patients. Brain, 123(Pt 2), 291\u2013307.","journal-title":"Brain"},{"issue":"4","key":"9_CR4","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1086\/429131","volume":"76","author":"N. Cope","year":"2005","unstructured":"Cope, N., Harold, D., Hill, G., Moskvina, V., Stevenson, J., Holmans, P., et al. (2005). Strong evidence that kiaa0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. American Journal of Human Genetics, 76(4), 581\u2013591.","journal-title":"American Journal of Human Genetics"},{"issue":"2","key":"9_CR5","doi-asserted-by":"crossref","first-page":"128","DOI":"10.1007\/s00439-004-1126-6","volume":"115","author":"K. E. Deffenbacher","year":"2004","unstructured":"Deffenbacher, K. E., Kenyon, J. B., Hoover, D. M., Olson, R. K., Pennington, B. F., DeFries, J. C., et al. (2004). Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: Linkage and association analyses. Human Genetics, 115(2), 128\u2013138.","journal-title":"Human Genetics"},{"issue":"7","key":"9_CR6","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1016\/j.tics.2005.05.004","volume":"9","author":"S. Dehaene","year":"2005","unstructured":"Dehaene, S., Cohen, L., Sigman, M., & Vinckier, F. (2005). The neural code for written words: A proposal. Trends in Cognitive Sciences, 9(7), 335\u2013341.","journal-title":"Trends in Cognitive Sciences"},{"issue":"3","key":"9_CR7","doi-asserted-by":"crossref","first-page":"198","DOI":"10.1002\/1098-2779(2000)6:3<198::AID-MRDD7>3.0.CO;2-1","volume":"6","author":"M. A. Eckert","year":"2000","unstructured":"Eckert, M. A., & Leonard, C. M. (2000). Structural imaging in dyslexia: The planum temporale. Mental Retardation and Developmental Disabilility Research Review, 6(3), 198\u2013206.","journal-title":"Mental Retardation and Developmental Disabilility Research Review"},{"issue":"1","key":"9_CR8","doi-asserted-by":"crossref","first-page":"146","DOI":"10.1086\/302190","volume":"64","author":"S. E. Fisher","year":"1999","unstructured":"Fisher, S. E., Marlow, A. J., Lamb, J., Maestrini, E., Williams, D. F., Richardson, A. J., et al. (1999). A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. American Journal of Human Genetics, 64(1), 146\u2013156.","journal-title":"American Journal of Human Genetics"},{"issue":"2","key":"9_CR9","doi-asserted-by":"crossref","first-page":"404","DOI":"10.1037\/0735-7044.111.2.404","volume":"111","author":"R. H. Fitch","year":"1997","unstructured":"Fitch, R. H., Brown, C. P., Tallal, P., & Rosen, G. D. (1997). Effects of sex and mk-801 on auditory-processing deficits associated with developmental microgyric lesions in rats. Behavioral Neuroscience, 111(2), 404\u2013412.","journal-title":"Behavioral Neuroscience"},{"issue":"6","key":"9_CR10","doi-asserted-by":"crossref","first-page":"1046","DOI":"10.1086\/426404","volume":"75","author":"C. Francks","year":"2004","unstructured":"Francks, C., Paracchini, S., Smith, S. D., Richardson, A. J., Scerri, T. S., Cardon, L. R., et al. (2004). A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. American Journal of Human Genetics, 75(6), 1046\u20131058.","journal-title":"American Journal of Human Genetics"},{"issue":"2","key":"9_CR11","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1016\/j.devbrainres.2004.06.007","volume":"152","author":"J. T. Friedman","year":"2004","unstructured":"Friedman, J. T., Peiffer, A. M., Clark, M. G., Benasich, A. A., & Fitch, R. H. (2004). Age and experience-related improvements in gap detection in the rat. Brain Research. Developmental Brain Research, 152(2), 83\u201391.","journal-title":"Brain Research. Developmental Brain Research"},{"issue":"1\u20133","key":"9_CR12","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1016\/0010-0277(94)90025-6","volume":"50","author":"A. M. Galaburda","year":"1994","unstructured":"Galaburda, A. M. (1994). Developmental dyslexia and animal studies: At the interface between cognition and neurology. Cognition, 50(1\u20133), 133\u2013149.","journal-title":"Cognition"},{"key":"9_CR13","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1002\/ana.410060203","volume":"6","author":"A. M. Galaburda","year":"1979","unstructured":"Galaburda, A. M., & Kemper, T. L. (1979). Cytoarchitectonic abnormalities in developmental dyslexia: A case study. Annals of Neurology, 6, 94\u2013100.","journal-title":"Annals of Neurology"},{"key":"9_CR14","doi-asserted-by":"crossref","first-page":"852","DOI":"10.1126\/science.341314","volume":"199","author":"A. M. Galaburda","year":"1978","unstructured":"Galaburda, A. M., LeMay, M., Kemper, T. L., & Geschwind, N. (1978). Right-left asymmetries in the brain. Science, 199, 852\u2013856.","journal-title":"Science"},{"key":"9_CR15","doi-asserted-by":"crossref","first-page":"222","DOI":"10.1002\/ana.410180210","volume":"18","author":"A. M. Galaburda","year":"1985","unstructured":"Galaburda, A. M., Sherman, G. F., Rosen, G. D., Aboitiz, F., & Geschwind, N. (1985). Developmental dyslexia: Four consecutive cases with cortical anomalies. Annals of Neurology, 18, 222\u2013233.","journal-title":"Annals of Neurology"},{"key":"9_CR16","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1007\/BF02647951","volume":"23","author":"N. Geschwind","year":"1982","unstructured":"Geschwind, N. (1982). Why Orton was right. Annals of Dyslexia, 23, 13\u201330.","journal-title":"Annals of Dyslexia"},{"key":"9_CR17","doi-asserted-by":"crossref","first-page":"428","DOI":"10.1001\/archneur.1985.04060050026008","volume":"42","author":"N. Geschwind","year":"1985","unstructured":"Geschwind, N., & Galaburda, A. M. (1985a). Cerebral lateralization. Biological mechanisms, associations, and pathology: I. A hypothesis and a program for research. Archives of Neurology, 42, 428\u2013462.","journal-title":"Archives of Neurology"},{"key":"9_CR18","doi-asserted-by":"crossref","first-page":"521","DOI":"10.1001\/archneur.1985.04060060019009","volume":"42","author":"N. Geschwind","year":"1985","unstructured":"Geschwind, N., & Galaburda, A. M. (1985b). Cerebral lateralization. Biological mechanisms, associations, and pathology: II. A hypothesis and a program for research. Archives of Neurology, 42, 521\u2013556.","journal-title":"Archives of Neurology"},{"key":"9_CR19","doi-asserted-by":"crossref","first-page":"634","DOI":"10.1001\/archneur.1985.04060070024012","volume":"42","author":"N. Geschwind","year":"1985","unstructured":"Geschwind, N., & Galaburda, A. M. (1985c). Cerebral lateralization. Biological mechanisms, associations, and pathology: III. A hypothesis and a program for research. Archives of Neurology, 42, 634\u2013654.","journal-title":"Archives of Neurology"},{"key":"9_CR20","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1126\/science.161.3837.186","volume":"161","author":"N. Geschwind","year":"1968","unstructured":"Geschwind, N., & Levitsky, W. (1968). Human brain: Left-right asymmetries in temporal speech region. Science, 161, 186\u2013187.","journal-title":"Science"},{"issue":"1","key":"9_CR21","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1111\/1469-7610.00704","volume":"42","author":"E. L. Grigorenko","year":"2001","unstructured":"Grigorenko, E. L. (2001). Developmental dyslexia: An update on genes, brains, and environments. Journal of Child Psychology and Psychiatry, 42(1), 91\u2013125.","journal-title":"Journal of Child Psychology and Psychiatry"},{"issue":"1","key":"9_CR22","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1002\/ajmg.b.10032","volume":"118","author":"E. L. Grigorenko","year":"2003","unstructured":"Grigorenko, E. L., Wood, F. B., Golovyan, L., Meyer, M., Romano, C., & Pauls, D. (2003). Continuing the search for dyslexia genes on 6p. American Journal of Medical Genetics. Part B, Neuropsychiatrics Genetics, 118(1), 89\u201398.","journal-title":"American Journal of Medical Genetics. Part B, Neuropsychiatrics Genetics"},{"issue":"2","key":"9_CR23","doi-asserted-by":"crossref","first-page":"715","DOI":"10.1086\/302755","volume":"66","author":"E. L. Grigorenko","year":"2000","unstructured":"Grigorenko, E. L., Wood, F. B., Meyer, M. S., & Pauls, D. L. (2000). Chromosome 6p influences on different dyslexia-related cognitive processes: Further confirmation. American Journal of Human Genetics, 66(2), 715\u2013723.","journal-title":"American Journal of Human Genetics"},{"issue":"5587","key":"9_CR24","doi-asserted-by":"crossref","first-page":"1660","DOI":"10.1126\/science.1074572","volume":"297","author":"M. E. Hatten","year":"2002","unstructured":"Hatten, M. E. (2002). New directions in neuronal migration. Science, 297(5587), 1660\u20131663.","journal-title":"Science"},{"issue":"5","key":"9_CR25","doi-asserted-by":"crossref","first-page":"453","DOI":"10.1093\/cercor\/7.5.453","volume":"7","author":"A. E. Herman","year":"1997","unstructured":"Herman, A. E., Galaburda, A. M., Fitch, R. H., Carter, A. R., & Rosen, G. D. (1997). Cerebral microgyria, thalamic cell size and auditory temporal processing in male and female rats. Cerebral Cortex, 7(5), 453\u2013464.","journal-title":"Cerebral Cortex"},{"issue":"2","key":"9_CR26","doi-asserted-by":"crossref","first-page":"238","DOI":"10.1212\/WNL.39.2.238","volume":"39","author":"W. E. Kaufmann","year":"1989","unstructured":"Kaufmann, W. E., & Galaburda, A. M. (1989). Cerebrocortical microdysgenesis in neurologically normal subjects: A histopathologic study. Neurology, 39(2), 238\u2013244.","journal-title":"Neurology"},{"issue":"1","key":"9_CR27","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1186\/1471-2164-4-25","volume":"4","author":"E. R. Londin","year":"2003","unstructured":"Londin, E. R., Meng, H., & Gruen, J. R. (2003). A transcription map of the 6p22.3 reading disability locus identifying candidate genes. BMC Genomics, 4(1), 25.","journal-title":"BMC Genomics"},{"key":"9_CR28","first-page":"139","volume-title":"Language, communication and the brain","author":"H. A. Lubs","year":"1988","unstructured":"Lubs, H. A., Smith, S., Kimberling, W., Pennington, B., Gross-Glenn, K., & Duara, R. (1988). Dyslexia sybtypes: Genetics, behavior, and brain imaging. In F. Plum (Ed.), Language, communication and the brain (pp. 139\u2013147). New York: Raven Press."},{"issue":"4","key":"9_CR29","doi-asserted-by":"crossref","first-page":"198","DOI":"10.1007\/s00787-003-0332-4","volume":"12","author":"C. Marino","year":"2003","unstructured":"Marino, C., Giorda, R., Vanzin, L., Molteni, M., Lorusso, M. L., Nobile, M., et al. (2003). No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes. European Journal of Child and Adolescent Psychiatry: Acta Paedopsychiatrica, 12(4), 198\u2013202.","journal-title":"European Journal of Child and Adolescent Psychiatry: Acta Paedopsychiatrica"},{"issue":"4","key":"9_CR30","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1016\/j.ijdevneu.2004.12.008","volume":"23","author":"M. M. McClure","year":"2005","unstructured":"McClure, M. M., Peiffer, A. M., Rosen, G. D., & Fitch, R. H. (2005). Auditory processing deficits in rats with neonatal hypoxic-ischemic injury. International Journal of Developmental Neuroscience, 23(4), 351\u2013362.","journal-title":"International Journal of Developmental Neuroscience"},{"issue":"4","key":"9_CR31","doi-asserted-by":"crossref","first-page":"280","DOI":"10.1177\/08830738050200040301","volume":"20","author":"M. F. McManus","year":"2005","unstructured":"McManus, M. F., & Golden, J. A. (2005). Neuronal migration in developmental disorders. Journal of Child Neurology, 20(4), 280\u2013286.","journal-title":"Journal of Child Neurology"},{"key":"9_CR32","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1001\/archneurpsyc.1925.02200170002001","volume":"14","author":"S. T. Orton","year":"1925","unstructured":"Orton, S. T. (1925). \u201cWord-blindness\u201d in school children. Archives of Neurology and Psychiatry, 14, 581\u2013615.","journal-title":"Archives of Neurology and Psychiatry"},{"issue":"13","key":"9_CR33","doi-asserted-by":"crossref","first-page":"2875","DOI":"10.1097\/00001756-200109170-00024","volume":"12","author":"A. M. Peiffer","year":"2001","unstructured":"Peiffer, A. M., Dunleavy, C. K., Frenkel, M., Gabel, L. A., LoTurco, J. J., Rosen, G. D., et al. (2001). Impaired detection of variable duration embedded tones in ectopic nzb\/binj mice. Neuroreport, 12(13), 2875\u20132879.","journal-title":"Neuroreport"},{"issue":"2","key":"9_CR34","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1016\/j.devbrainres.2004.06.003","volume":"152","author":"A. M. Peiffer","year":"2004","unstructured":"Peiffer, A. M., Friedman, J. T., Rosen, G. D., & Fitch, R. H. (2004a). Impaired gap detection in juvenile microgyric rats. Brain Research. Developmental Brain Research, 152(2), 93\u201398.","journal-title":"Brain Research. Developmental Brain Research"},{"issue":"12","key":"9_CR35","doi-asserted-by":"crossref","first-page":"1923","DOI":"10.1097\/00001756-200408260-00018","volume":"15","author":"A. M. Peiffer","year":"2004","unstructured":"Peiffer, A. M., McClure, M. M., Threlkeld, S. W., Rosen, G. D., & Fitch, R. H. (2004b). Severity of focal microgyria and associated rapid auditory processing deficits. Neuroreport, 15(12), 1923\u20131926.","journal-title":"Neuroreport"},{"issue":"2","key":"9_CR36","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1016\/S0165-3806(02)00472-8","volume":"138","author":"A. M. Peiffer","year":"2002","unstructured":"Peiffer, A. M., Rosen, G. D., & Fitch, R. H. (2002a). Rapid auditory processing and mgn morphology in microgyric rats reared in varied acoustic environments. Brain Research. Developmental Brain Research, 138(2), 187\u2013193.","journal-title":"Brain Research. Developmental Brain Research"},{"issue":"17","key":"9_CR37","doi-asserted-by":"crossref","first-page":"2277","DOI":"10.1097\/00001756-200212030-00021","volume":"13","author":"A. M. Peiffer","year":"2002","unstructured":"Peiffer, A. M., Rosen, G. D., & Fitch, R. H. (2002b). Sex differences in rapid auditory processing deficits in ectopic bxsb\/mpj mice. Neuroreport, 13(17), 2277\u20132280.","journal-title":"Neuroreport"},{"issue":"1","key":"9_CR38","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1016\/j.devbrainres.2003.09.020","volume":"148","author":"A. M. Peiffer","year":"2004","unstructured":"Peiffer, A. M., Rosen, G. D., & Fitch, R. H. (2004c). Sex differences in rapid auditory processing deficits in microgyric rats. Brain Research. Developmental Brain Research, 148(1), 53\u201357.","journal-title":"Brain Research. Developmental Brain Research"},{"issue":"2\/3","key":"9_CR39","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1006\/ccog.1997.0301","volume":"6","author":"M. I. Posner","year":"1997","unstructured":"Posner, M. I., DiGirolamo, G. J., & Fernandez-Duque, D. (1997). Brain mechanisms of cognitive skills. Conscious Cognition, 6(2\/3), 267\u2013290.","journal-title":"Conscious Cognition"},{"issue":"12","key":"9_CR40","doi-asserted-by":"crossref","first-page":"720","DOI":"10.1016\/j.tins.2004.10.004","volume":"27","author":"F. Ramus","year":"2004","unstructured":"Ramus, F. (2004). Neurobiology of dyslexia: A reinterpretation of the data. Trends in Neurosciences, 27(12), 720\u2013726.","journal-title":"Trends in Neurosciences"},{"key":"9_CR41","doi-asserted-by":"crossref","first-page":"237","DOI":"10.3109\/00207458908987438","volume":"47","author":"G. D. Rosen","year":"1989","unstructured":"Rosen, G. D., Galaburda, A. M., & Sherman, G. F. (1989). Cerebrocortical microdysgenesis with anomalous callosal connections: A case study in the rat. International Journal of Neuroscence, 47, 237\u2013247.","journal-title":"International Journal of Neuroscence"},{"issue":"1","key":"9_CR42","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1093\/cercor\/9.1.27","volume":"9","author":"G. D. Rosen","year":"1999","unstructured":"Rosen, G. D., Herman, B. A., & Galaburda, A. M. (1999). Sex differences in the effects of early neocortical injury on neuronal size distribution of the medial geniculate nucleus in the rat are mediated by perinatal gonadal steroids. Cerebral Cortex, 9(1), 27\u201334.","journal-title":"Cerebral Cortex"},{"issue":"6","key":"9_CR43","doi-asserted-by":"crossref","first-page":"601","DOI":"10.1097\/00005072-199211000-00005","volume":"51","author":"G. D. Rosen","year":"1992","unstructured":"Rosen, G. D., Press, D. M., Sherman, G. F., & Galaburda, A. M. (1992). The development of induced cerebrocortical microgyria in the rat. Journal of Neuropathology and Experimental Neurology, 51(6), 601\u2013611.","journal-title":"Journal of Neuropathology and Experimental Neurology"},{"key":"9_CR44","doi-asserted-by":"crossref","first-page":"525","DOI":"10.1016\/0306-4522(89)90404-1","volume":"33","author":"G. D. Rosen","year":"1989","unstructured":"Rosen, G. D., Sherman, G. F., & Galaburda, A. M. (1989). Interhemispheric connections differ between symmetrical and asymmetrical brain regions. Neuroscience, 33, 525\u2013533.","journal-title":"Neuroscience"},{"issue":"11","key":"9_CR45","doi-asserted-by":"crossref","first-page":"853","DOI":"10.1136\/jmg.2004.018341","volume":"41","author":"T. S. Scerri","year":"2004","unstructured":"Scerri, T. S., Fisher, S. E., Francks, C., MacPhie, I. L., Paracchini, S., Richardson, A. J., et al. (2004). Putative functional alleles of dyx1c1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. Journal of Medical Genetics, 41(11), 853\u2013857.","journal-title":"Journal of Medical Genetics"},{"issue":"5","key":"9_CR46","doi-asserted-by":"crossref","first-page":"433","DOI":"10.1007\/s11910-003-0027-8","volume":"3","author":"V. L. Sheen","year":"2003","unstructured":"Sheen, V. L., & Walsh, C. A. (2003). Developmental genetic malformations of the cerebral cortex. Current Neurology and Neuroscience Reports, 3(5), 433\u2013441.","journal-title":"Current Neurology and Neuroscience Reports"},{"key":"9_CR47","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1016\/0006-8993(90)91737-2","volume":"532","author":"G. F. Sherman","year":"1990","unstructured":"Sherman, G. F., Morrison, L., Rosen, G. D., Behan, P. O., & Galaburda, A. M. (1990). Brain abnormalities in immune defective mice. Brain Research, 532, 25\u201333.","journal-title":"Brain Research"},{"key":"9_CR48","doi-asserted-by":"crossref","first-page":"202","DOI":"10.1016\/0006-8993(90)90828-Y","volume":"529","author":"G. F. Sherman","year":"1990","unstructured":"Sherman, G. F., Stone, J. S., Press, D. M., Rosen, G. D., & Galaburda, A. M. (1990). Abnormal architecture and connections disclosed by neurofilament staining in the cerebral cortex of autoimmune mice. Brain Research, 529, 202\u2013207.","journal-title":"Brain Research"},{"key":"9_CR49","first-page":"1133","volume":"27","author":"G. F. Sherman","year":"1997","unstructured":"Sherman, G. F., Stone, L. V., Galaburda, A. M., & Beier, D. R. (1997). Linkage analysis of neurocortical ectopias in nxsm-d mice. Society for Neuroscience Abstracts, 27, 1133.","journal-title":"Society for Neuroscience Abstracts"},{"key":"9_CR50","doi-asserted-by":"crossref","first-page":"1345","DOI":"10.1126\/science.6828864","volume":"219","author":"S. D. Smith","year":"1983","unstructured":"Smith, S. D., Kimberling, W. J., Pennington, B. F., & Lubs, H. A. (1983). Specific reading disability: Identification of an inherited form through linkage analysis. Science, 219, 1345\u20131347.","journal-title":"Science"},{"issue":"20","key":"9_CR51","doi-asserted-by":"crossref","first-page":"11553","DOI":"10.1073\/pnas.1833911100","volume":"100","author":"M. Taipale","year":"2003","unstructured":"Taipale, M., Kaminen, N., Nopola-Hemmi, J., Haltia, T., Myllyluoma, B., Lyytinen, H., et al. (2003). A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proceedings of the National Academy of Sciences of the United States of America, 100(20), 11553\u201311558.","journal-title":"Proceedings of the National Academy of Sciences of the United States of America"},{"key":"9_CR52","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1038\/241468a0","volume":"241","author":"P. Tallal","year":"1973","unstructured":"Tallal, P., & Piercy, M. (1973). Defects of non-verbal auditory perception in children with developmental aphasia. Nature, 241, 468\u2013469.","journal-title":"Nature"},{"issue":"12","key":"9_CR53","doi-asserted-by":"crossref","first-page":"1111","DOI":"10.1038\/sj.mp.4001543","volume":"9","author":"K. G. Wigg","year":"2004","unstructured":"Wigg, K. G., Couto, J. M., Feng, Y., Anderson, B., Cate-Carter, T. D., Macciardi, F., et al. (2004). Support for ekn1 as the susceptibility locus for dyslexia on 15q21. Molecular Psychiatry, 9(12), 1111\u20131121.","journal-title":"Molecular Psychiatry"},{"issue":"1","key":"9_CR54","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1038\/sj.ejhg.5201272","volume":"13","author":"T. Ylisaukko-Oja","year":"2005","unstructured":"Ylisaukko-Oja, T., Peyrard-Janvid, M., Lindgren, C. M., Rehnstrom, K., Vanhala, R., Peltonen, L., et al. (2005). Family-based association study of dyx1c1 variants in autism. European Journal of Human Genetics, 13(1), 127\u2013130.","journal-title":"European Journal of Human Genetics"}],"container-title":["Annals of Dyslexia"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s11881-005-0009-4.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s11881-005-0009-4\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s11881-005-0009-4","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,6,1]],"date-time":"2019-06-01T23:38:25Z","timestamp":1559432305000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s11881-005-0009-4"}},"subtitle":["The 2004 Norman Geschwind memorial lecture"],"short-title":[],"issued":{"date-parts":[[2005,12]]},"references-count":54,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2005,12]]}},"alternative-id":["9"],"URL":"https:\/\/doi.org\/10.1007\/s11881-005-0009-4","relation":{},"ISSN":["0736-9387","1934-7243"],"issn-type":[{"value":"0736-9387","type":"print"},{"value":"1934-7243","type":"electronic"}],"subject":[],"published":{"date-parts":[[2005,12]]}}}