The 42 references in paper E. Malinina V., I. Zabozlaeva V., Е. Малинина В., И. Забозлаева В. (2016) “Синдром Ретта: трудности диагностики (клинико-психопатологические аспекты) // RETT SYNDROME: DIFFICULTIES OF DIAGNOSTICS (CLINICAL AND PSYCHOPATHOLOGICAL ASPECTS)” / spz:neicon:rjdn:y:2016:i:3:p:49-56

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Ворсанова С.Г., Юров Ю.Б., Сильванович А.П. и др. Современные представления о молекулярной генетике и геномике аутизма. Фундаментальные исследования 2013;4(2):356–67. [Vorsanovа S.G., Yurov Yu.B., Sil’vanovich А.P. et al. Modern perceptions of the molecular genetics and autism genomics. Fundamental’nye issledovaniya = Fundamental Studies 2013;4(2):356–67. (In Russ.)].
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Ворсанова С.Г., Юров И.Ю., Воинова В.Ю. и др. Микроделеционные формы синдрома Ретта, выявленные методом молекулярного кариотипирования на ДНК-микроматрицах (array CGH), у девочек без мутаций в гене MECP2. Журнал неврологии и психиатрии им. С.С. Корсакова 2013;113(10): 47–52. [Vorsanovа S.G., Yurov I.Yu., Voinovа V.Yu. et al. Мicrodeletion forms of the Rett’s syndrome, revealed by the molecular caryotyping method on DNAmatrices (array CGH), at girls without mutations in the MECP2 gene. Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova = S.S. Korsakov Journal of Neurology and Psychiatry 2013;113(10):47–52. (In Russ.)].
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Ворсанова С.Г., Юров И.Ю., Куринная О.С. и др. Молекулярное кариотипирование: проблемы диагностики моногенных заболеваний без выявленных мутаций на примере синдромов аутистических расстройств (синдром Ретта). Фундаментальные исследования 2014;11(2):324–8. [Vorsanovа S.G., Yurov I.Yu., Kurinnaya О.S. et al. Моlecular caryotyping: problems of diagnostics of monogenic diseases without revealed mutations at the example of syndromes of autistic diseases (Rett’s syndrome). Fundamental’nye issledovaniya = Fundamental Studies 2014;11(2):324–8. (In Russ.)].
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