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Volumn 96, Issue 49, 1999, Pages 5488-5490

Rett syndrome, an odd disorder affecting girls; update of 25-year follow-up in western Sweden;Retts syndrom - Ett egenartat handikapp som drabbar flicker: Aktuell västsvensk uppföljning genom 25 år

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; FEMALE; FOLLOW UP; GENETICS; HUMAN; MIDDLE AGED; MORTALITY; PRESCHOOL CHILD; PROGNOSIS; RETT SYNDROME; SWEDEN;

EID: 0033536967     PISSN: 00237205     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (17)
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  • 3
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    • Rett variants: A suggested model for inclusion criteria
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    • Hagberg, B.1    Skjeldal, O.H.2
  • 5
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    • A progressive syndrome of autism, dementia, ataxia and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
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    • (1983) Ann Neurol , vol.14 , pp. 471-479
    • Hagberg, B.1    Aicardi, J.2    Dias, K.3    Ramos, O.4
  • 8
    • 0032945641 scopus 로고    scopus 로고
    • Altered development of glutamate receptors in frontal cortex from girls with Rett syndrome
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  • 11
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  • 12
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    • The genetic basis of Rett syndrome: Candidate gene considerations
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    • Percy, A.K.1    Schanen, C.2    Dure, L.S.3
  • 13
    • 17344364662 scopus 로고    scopus 로고
    • Chromosome mapping of Rett syndrome: A likely candidate region on the telomere of Xq
    • Xiang F, Zhang Z, Clarke A, Joseluiz P, Naidu S, Budden S et al. Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq. J Med Genet 1998; 35: 297-300.
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  • 14
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  • 15
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  • 17
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    • Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
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    • Amir, R.E.1    Van Den Veyver, I.B.2    Wan, M.3    Tran, C.Q.4    Francke, U.5    Zoghbi, H.Y.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.