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Titlebook: Reading Disabilities; Genetic and Neurolog Bruce F. Pennington Book 1991 Springer Science+Business Media Dordrecht 1991 behavior.brain.cogn

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發(fā)表于 2025-3-21 20:04:04 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Reading Disabilities
副標(biāo)題Genetic and Neurolog
編輯Bruce F. Pennington
視頻videohttp://file.papertrans.cn/822/821943/821943.mp4
叢書名稱Neuropsychology and Cognition
圖書封面Titlebook: Reading Disabilities; Genetic and Neurolog Bruce F. Pennington Book 1991 Springer Science+Business Media Dordrecht 1991 behavior.brain.cogn
描述This book is unique in that it brings together in one place anaccount of recent advances in our understanding of the biology ofdyslexia. It grew out of a Rodin Remediation Foundation Internationalconference held on this topic in Boulder, Colorado in 1990, whichincluded most of the world‘s experts on the genetics and neurology ofdyslexia. Ten years ago a volume on this topic would scarcely beenpossible, and now we have an emerging, comprehensive neuroscientificunderstanding of this complex behavioral disorder that goes from genesto brain to behavior. Building on recent advances in the understandingof the cognitive phenotype of dyslexia, these authors present new dataon both the etiology and brain mechanisms underlying that phenotype.Reading disability or dyslexia has a high familial recurrence rate,and is partly heritable. Genetic linkage studies are beginning toidentify the possible locations of genes influencing this phenotype.On the neurological side, several independent studies have foundneuroanatomical differences in the dyslexic brain, which are due toearly changes in brain development. Thus, contrary to the views heldby some educators that dyslexia is a myth, the results pres
出版日期Book 1991
關(guān)鍵詞behavior; brain; cognition; family studies; neurology; neuropathology; neuropsychology; psychology
版次1
doihttps://doi.org/10.1007/978-94-011-2450-8
isbn_softcover978-94-010-5081-4
isbn_ebook978-94-011-2450-8Series ISSN 0927-0116
issn_series 0927-0116
copyrightSpringer Science+Business Media Dordrecht 1991
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 21:08:53 | 只看該作者
https://doi.org/10.1007/978-94-011-2450-8behavior; brain; cognition; family studies; neurology; neuropathology; neuropsychology; psychology
板凳
發(fā)表于 2025-3-22 01:37:46 | 只看該作者
Genetic and Neurological Influences on Reading Disability: An Overviewvoted to the topic of genetic and neurological influences on dyslexia, or reading disability (RD). This conference would not have been possible without the vision and generosity of Per Udden and the Rodin Remediation Foundation, who have been unique catalysts in fostering an interdisciplinary understanding of dyslexia or RD.
地板
發(fā)表于 2025-3-22 05:30:31 | 只看該作者
978-94-010-5081-4Springer Science+Business Media Dordrecht 1991
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發(fā)表于 2025-3-22 15:54:19 | 只看該作者
0927-0116 grew out of a Rodin Remediation Foundation Internationalconference held on this topic in Boulder, Colorado in 1990, whichincluded most of the world‘s experts on the genetics and neurology ofdyslexia. Ten years ago a volume on this topic would scarcely beenpossible, and now we have an emerging, compr
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發(fā)表于 2025-3-22 17:30:42 | 只看該作者
Which Aspects of Processing Text Mediate Genetic Effects?of h... In contrast measures of Phonological Coding and Homophone Recognition have consistently high values of h... More detailed analyses suggested that there were possibly two independent aspects of phonological ability, each influenced by genetic factors.
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發(fā)表于 2025-3-23 00:17:05 | 只看該作者
Genetic Etiology of Spelling Deficits in the Colorado and London Twin Studies of Reading Disabilitymates of h.. were 0.66 ±0.18 and 0.56 ± 0.19, respectively, a nonsignificant difference. Collaborative analyses of data from additional twin studies of reading disability would facilitate more rigorous tests of hypotheses of differential genetic etiology as a function of group membership.
9#
發(fā)表于 2025-3-23 03:38:29 | 只看該作者
Screening for Multiple Genes Influencing Dyslexias studies (with less than 200 sib pairs) and two different means of diagnosis of dyslexia, the sib pair analysis was able to detect the same suggested linkages as the LOD score method, plus a possible third region. This confirms that the sib pair method is an effective means of screening for linkage with reasonable sample sizes.
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發(fā)表于 2025-3-23 05:47:38 | 只看該作者
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