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Volumn 2007, Issue , 2007, Pages

Tetrasomy 15q11-q13 diagnosed by FISH in a patient with autistic disorder

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BEHAVIOR DISORDER; CASE REPORT; CHILD; CHROMOSOME 15; CHROMOSOME 15Q; CHROMOSOME ANALYSIS; CLINICAL FEATURE; CYTOGENETICS; DEVELOPMENTAL DISORDER; EPILEPSY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HYPERACTIVITY; INFANTILE AUTISM; MALE; MARKER CHROMOSOME; MENTAL DEFICIENCY; SUPERNUMERARY CHROMOSOME; TETRASOMY;

EID: 34247219710     PISSN: 11107243     EISSN: 11107251     Source Type: Journal    
DOI: 10.1155/2007/61538     Document Type: Article
Times cited : (6)

References (11)
  • 2
    • 0027934165 scopus 로고
    • Brief report: Duplication of chromosome 15q11-13 in two individuals with autistic disorder
    • P. Baker J. Piven S. Schwartz S. Patil Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder. Journal of Autism and Developmental Disorders 24 4 1994 529 535
    • (1994) Journal of Autism and Developmental Disorders , vol.24 , Issue.4 , pp. 529-535
    • Baker, P.1    Piven, J.2    Schwartz, S.3    Patil, S.4
  • 5
    • 22244476747 scopus 로고    scopus 로고
    • The inv dup(15) or idic(15) syndrome: A clinically recognisable neurogenetic disorder
    • abattaglia@inpe.unipi.it. Epub April 2005
    • A. Battaglia abattaglia@inpe.unipi.it The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder. Brain and Development 27 5 2005 365 369 Epub April 2005
    • (2005) Brain and Development , vol.27 , Issue.5 , pp. 365-369
    • Battaglia, A.1
  • 7
    • 0242607218 scopus 로고    scopus 로고
    • Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity
    • ser@soton.ac.uk f.maggouta@dial.pipex.com. Epub October 2003
    • S. E. Roberts ser@soton.ac.uk F. Maggouta f.maggouta@dial.pipex.com N. S. Thomas P. A. Jacobs J. A. Crolla Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity. American Journal of Human Genetics 73 5 2003 1061 1072 Epub October 2003
    • (2003) American Journal of Human Genetics , vol.73 , Issue.5 , pp. 1061-1072
    • Roberts, S.E.1    Maggouta, F.2    Thomas, N.S.3    Jacobs, P.A.4    Crolla, J.A.5
  • 9
    • 0035417396 scopus 로고    scopus 로고
    • Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families
    • E. L. Nurmi Y. Bradford Y.-H. Chen Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. Genomics 77 1-2 2001 105 113
    • (2001) Genomics , vol.77 , Issue.1-2 , pp. 105-113
    • Nurmi, E.L.1    Bradford, Y.2    Chen, Y.-H.3
  • 10
    • 4644285329 scopus 로고    scopus 로고
    • Molecular genetics of autism spectrum disorder
    • ed@yoda.bsd.uchicago.edu
    • J. Veenstra-VanderWeele E. H. Cook Jr. ed@yoda.bsd.uchicago.edu Molecular genetics of autism spectrum disorder. Molecular Psychiatry 9 9 2004 819 832
    • (2004) Molecular Psychiatry , vol.9 , Issue.9 , pp. 819-832
    • Veenstra-Vanderweele, J.1    Cook Jr., E.H.2
  • 11
    • 0033652564 scopus 로고    scopus 로고
    • Isolation and molecular analysis of inv dup(15) and construction of a physical map of a common breakpoint in order to elucidate their mechanism of formation
    • A. E. Wandstrat S. Schwartz Isolation and molecular analysis of inv dup(15) and construction of a physical map of a common breakpoint in order to elucidate their mechanism of formation. Chromosoma 109 7 2000 498 505
    • (2000) Chromosoma , vol.109 , Issue.7 , pp. 498-505
    • Wandstrat, A.E.1    Schwartz, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.