標(biāo)題: Titlebook: Genetics and Genomics of Neurobehavioral Disorders; Gene S. Fisch (Senior Research Scientist) Book 2003 Springer Science+Business Media Ne [打印本頁] 作者: 柳條筐 時(shí)間: 2025-3-21 18:07
書目名稱Genetics and Genomics of Neurobehavioral Disorders影響因子(影響力)
書目名稱Genetics and Genomics of Neurobehavioral Disorders影響因子(影響力)學(xué)科排名
書目名稱Genetics and Genomics of Neurobehavioral Disorders網(wǎng)絡(luò)公開度
書目名稱Genetics and Genomics of Neurobehavioral Disorders網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Genetics and Genomics of Neurobehavioral Disorders被引頻次
書目名稱Genetics and Genomics of Neurobehavioral Disorders被引頻次學(xué)科排名
書目名稱Genetics and Genomics of Neurobehavioral Disorders年度引用
書目名稱Genetics and Genomics of Neurobehavioral Disorders年度引用學(xué)科排名
書目名稱Genetics and Genomics of Neurobehavioral Disorders讀者反饋
書目名稱Genetics and Genomics of Neurobehavioral Disorders讀者反饋學(xué)科排名
作者: SPER 時(shí)間: 2025-3-21 23:37 作者: absorbed 時(shí)間: 2025-3-22 03:27 作者: 全面 時(shí)間: 2025-3-22 04:36 作者: FUSC 時(shí)間: 2025-3-22 11:05
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作者: Flustered 時(shí)間: 2025-3-22 13:50 作者: Flustered 時(shí)間: 2025-3-22 20:33
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.作者: 階層 時(shí)間: 2025-3-22 21:17
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.作者: Lymphocyte 時(shí)間: 2025-3-23 03:01
Genetics and Genomics of Neurobehavioral Disorders作者: 制造 時(shí)間: 2025-3-23 08:51
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 作者: ferment 時(shí)間: 2025-3-23 12:14
Book 2003us 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作者: 不朽中國 時(shí)間: 2025-3-23 14:36 作者: Amorous 時(shí)間: 2025-3-23 19:40
Neuroanatomical Considerations Specific to the Study of Neurogeneticstical thinking, executive functions, visual cognition and mental imagery, and consciousness. These behaviors arise from intricate, developmental, and on-line interactions between genes and environment, having their ultimate effects at the molecular level. This understanding is difficult to achieve, 作者: 粗俗人 時(shí)間: 2025-3-24 00:42 作者: 規(guī)范要多 時(shí)間: 2025-3-24 06:10
What Can the Study of Behavioral Phenotypes Teach Us About the Pathway from Genes to Behavior? associated with mental retardation. As Hodapp and Dykens . report, there has been a 10-fold or greater increase in the number of articles published on the etiologies of genetic syndromes associated with mental retardation in the 1990s compared to the 1980s. The increase does not merely reflect adva作者: RODE 時(shí)間: 2025-3-24 06:36
Prader-Willi and Angelman Syndromesysical features. First identified 45 years ago, Prader—Willi syndrome (PWS) . is characterized by infantile hypotonia, hypogonadism, short stature, characteristic facial features, mild levels of cognitive delay, hyperphagia, increased risks of obesity, and obsessive—compulsive and other behavioral p作者: Occupation 時(shí)間: 2025-3-24 13:36
Tuberous Sclerosist many organs. Its manifestations are highly variable and include seizures, mental retardation, and a range of behavioral problems resulting from involvement of the central nervous system. Manifestations in the kidneys, heart, lungs, and skin are also of major clinical importance. Management should 作者: SOW 時(shí)間: 2025-3-24 15:51 作者: Amendment 時(shí)間: 2025-3-24 21:01 作者: 不容置疑 時(shí)間: 2025-3-25 00:08
Behavioral Phenotype in Myotonic Dystrophy (Steinert’s Disease)ut also the eye, heart, gastrointestinal tract, skin, immune system, endocrine system, skull, kidneys ., and brain .. Moreover, these systems may be affected differentially, the age at onset is variable, as well as the course of the disease. The severity of the disease tends to increase from one gen作者: Obsequious 時(shí)間: 2025-3-25 05:39 作者: 負(fù)擔(dān) 時(shí)間: 2025-3-25 10:08
ATR-X Syndromeia arises when there is a defect in the synthesis of the α-globin chains of adult hemoglobin (HbA, α2β2). When they described three mentally retarded children with α-thalassemia and a variety of developmental abnormalities, their interest was stimulated by the unusual nature of the α-thalassemia. Th作者: Temporal-Lobe 時(shí)間: 2025-3-25 13:02
The Fragile X Syndrome and the Fragile X Mutationenoted “a marker X chromosome” .. However, the report by Martin and Bell a generation earlier was the first to identify the disorder .. In their landmark paper, Martin and Bell describe a large pedigree in which “mentally deficient sons have been born to normally intelligent mothers.”作者: LITHE 時(shí)間: 2025-3-25 16:13 作者: Glutinous 時(shí)間: 2025-3-25 23:33
https://doi.org/10.1007/978-3-658-36780-0of at least part of the molecular basis of behavior, which has to do with the influence of hard-wired genetic factors. As before in the history of this field, the study of disorders, in this case genetic disorders, is a reasonable start.作者: 群島 時(shí)間: 2025-3-26 02:40 作者: 外露 時(shí)間: 2025-3-26 05:15 作者: Diluge 時(shí)間: 2025-3-26 08:36 作者: extinct 時(shí)間: 2025-3-26 15:03 作者: 反復(fù)拉緊 時(shí)間: 2025-3-26 17:24 作者: 雪上輕舟飛過 時(shí)間: 2025-3-26 23:39
Behavioral Phenotype in Velo-Cardio-Facial Syndromelted in the same deletion being linked to several syndromes including DiGeorge syndrome, conotruncal anomaly face syndrome, Cayler syndrome, and Opitz GBBB syndrome, and the term “22q11 deletion syndrome” has been proposed as a replacement term for these other designators.作者: pancreas 時(shí)間: 2025-3-27 04:41 作者: Adrenal-Glands 時(shí)間: 2025-3-27 08:40 作者: 羊欄 時(shí)間: 2025-3-27 11:41 作者: 祖?zhèn)?nbsp; 時(shí)間: 2025-3-27 17:18 作者: 詢問 時(shí)間: 2025-3-27 21:45 作者: 敬禮 時(shí)間: 2025-3-27 23:21 作者: Delirium 時(shí)間: 2025-3-28 03:51 作者: 槍支 時(shí)間: 2025-3-28 07:33
Williams-Beuren Syndromenvolving characteristic facial features, SVAS, and mental retardation .,.. Subsequent reports clearly demonstrated that the previously described clinical entities were the same, which might include a wider spectrum of abnormalities .,..作者: compel 時(shí)間: 2025-3-28 11:14 作者: Asymptomatic 時(shí)間: 2025-3-28 16:42 作者: 除草劑 時(shí)間: 2025-3-28 19:47 作者: 總 時(shí)間: 2025-3-29 01:52
Gene S. Fisch (Senior Research Scientist)Includes supplementary material: 作者: 影響 時(shí)間: 2025-3-29 05:42 作者: 反感 時(shí)間: 2025-3-29 08:14
https://doi.org/10.1007/978-3-658-36780-0tical thinking, executive functions, visual cognition and mental imagery, and consciousness. These behaviors arise from intricate, developmental, and on-line interactions between genes and environment, having their ultimate effects at the molecular level. This understanding is difficult to achieve, 作者: Cerumen 時(shí)間: 2025-3-29 12:39
https://doi.org/10.1007/978-3-8349-6321-5ited the completion of the human genome project, as this information will revolutionize modern medicine in ways that we are only starting to realize. Of immediate consequence is the enormous impact that the completed sequence will have on the lengthy and extremely laborious process of mapping and cl作者: conifer 時(shí)間: 2025-3-29 17:22 作者: 手榴彈 時(shí)間: 2025-3-29 23:21 作者: 弄臟 時(shí)間: 2025-3-30 02:32
https://doi.org/10.1007/978-3-663-04565-6t many organs. Its manifestations are highly variable and include seizures, mental retardation, and a range of behavioral problems resulting from involvement of the central nervous system. Manifestations in the kidneys, heart, lungs, and skin are also of major clinical importance. Management should 作者: 信徒 時(shí)間: 2025-3-30 04:59 作者: Yag-Capsulotomy 時(shí)間: 2025-3-30 12:11
https://doi.org/10.1007/978-3-322-88263-9gnitive and personality profiles, supravalvular aortic stenosis (SVAS), short stature, occasional transient hypercalcemia in infancy, and connective tissue anomalies .,.. It was first reported in 1952 under the name “idiopathic infantile hypercalcemia” as a syndrome defined by hypercalcemia, charact作者: 消瘦 時(shí)間: 2025-3-30 13:16
Arbeitereinsatz und Automatisierung,ut also the eye, heart, gastrointestinal tract, skin, immune system, endocrine system, skull, kidneys ., and brain .. Moreover, these systems may be affected differentially, the age at onset is variable, as well as the course of the disease. The severity of the disease tends to increase from one gen
