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Titlebook: Genetics and Genomics of Neurobehavioral Disorders; Gene S. Fisch (Senior Research Scientist) Book 2003 Springer Science+Business Media Ne

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發(fā)表于 2025-3-21 18:07:53 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Genetics and Genomics of Neurobehavioral Disorders
編輯Gene S. Fisch (Senior Research Scientist)
視頻videohttp://file.papertrans.cn/383/382700/382700.mp4
概述Includes supplementary material:
叢書名稱Contemporary Clinical Neuroscience
圖書封面Titlebook: Genetics and Genomics of Neurobehavioral Disorders;  Gene S. Fisch (Senior Research Scientist) Book 2003 Springer Science+Business Media Ne
描述In recent years, significant gains have been made in the cloning and identification of numerous genes that produce neurobehavioral disorders, as well as in the ability of neuropsychological tests to accurately assess and evaluate cognitive deficits and behavioral dysfunction. In Genetics and Genomics of Neurobehavioral Disorders, a panel of leading researchers draws on this new knowledge to provide a clear and comprehensive account of how genetic abnormalities, neurobiology, and neuropsychology work together to manifest cognitive-behavioral dysfunction. The authors review the current status of research in autosomal disorders that produce such dysfunctions, examining both microdeletion disorders (Prader-Willi syndrome/Angelman syndrome, deletion 22q11, and Williams syndrome) and syndromes arising from microdeletions and sequence variants, among them neurofibromatosis (NF1 and NF2), tuberous sclerosis (TSC1 and TSC2), and myotonic dystrophy. X-linked disorders producing mental retardation in syndromal disorders (ATRX, Rett, and fragile X) and nonsyndromal disorders (FRAXE and MRX) are also discussed. An insightful introduction surveys the history of neurobehavioral disorders, the est
出版日期Book 2003
關(guān)鍵詞Nervous System; Syndrom; genes; genetics; neurobiology; neuropsychology
版次1
doihttps://doi.org/10.1007/978-1-59259-353-8
isbn_softcover978-1-61737-322-0
isbn_ebook978-1-59259-353-8Series ISSN 2627-535X Series E-ISSN 2627-5341
issn_series 2627-535X
copyrightSpringer Science+Business Media New York 2003
The information of publication is updating

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https://doi.org/10.1007/978-3-663-08348-1genetic anomalies and the cognitive—behavioral deficits that result in difficulties in learning and memory, problem-solving, language, and other associated limitations in psychomotor development. That is not to say no other aspects of behavior may be affected. Various forms of psychopathology may de
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https://doi.org/10.1007/978-3-663-06802-0verse clinical manifestations. This conjecture has been confirmed, and what has emerged is the identification of two quite distinct syndromes: ATR-16, a contiguous gene syndrome and ATR-X, which results from mutation of a putative chromatin remodelling factor.
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https://doi.org/10.1007/978-3-663-06946-1have been found in most girls or women (and some boys) with RS. Surprisingly, mutations in this gene can also lead to a wide variety of clinical phenotypes ranging from normal females to fatal encephalopathy in males.
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Genetics and Genomics of Neurobehavioral Disorders
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2627-535X ndromal disorders (ATRX, Rett, and fragile X) and nonsyndromal disorders (FRAXE and MRX) are also discussed. An insightful introduction surveys the history of neurobehavioral disorders, the est978-1-61737-322-0978-1-59259-353-8Series ISSN 2627-535X Series E-ISSN 2627-5341
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