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Volumn 20, Issue 9, 2005, Pages 718-721

Rett syndrome: Model of neurodevelopmental disorders

Author keywords

[No Author keywords available]

Indexed keywords

BETAINE; FOLIC ACID; METHYL CPG BINDING PROTEIN 2;

EID: 27144493864     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/08830738050200090301     Document Type: Article
Times cited : (59)

References (16)
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  • 3
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    • Percy AK, Zoghbi H, Riccardi VM: Rett syndrome: Initial experience with an emerging clinical entity. Brain Dev 1985;7:300-304.
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    • Percy, A.K.1    Zoghbi, H.2    Riccardi, V.M.3
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    • Rett syndrome: Clinical experience in Alabama
    • Percy AK, Isaacs JS, Lane JB: Rett syndrome: Clinical experience in Alabama. Riv Med 1998;4:207-210.
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  • 6
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    • Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
    • Amir R, Van den Veyver I, Wan M, et al: Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 1999;23:185-188.
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    • Amir, R.1    Van Den Veyver, I.2    Wan, M.3
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    • Rett syndrome: Criteria for inclusion and exclusion
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    • Hagberg, B.1    Goutieres, F.2    Hanefeld, F.3
  • 8
    • 0023888966 scopus 로고
    • Diagnostic criteria for Rett syndrome
    • The Rett Syndrome Diagnostic Criteria Work Group
    • Diagnostic criteria for Rett syndrome. The Rett Syndrome Diagnostic Criteria Work Group. Ann Neurol 1988;23:425-428.
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  • 9
    • 0037002625 scopus 로고    scopus 로고
    • An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome Clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001
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  • 13
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    • Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: Implications for routine diagnosis of Rett syndrome
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  • 14
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    • Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.