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Volumn 43, Issue 6, 2010, Pages 391-394

Microarray analysis in children with developmental disorder or epilepsy

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; AUTISM; BODY DYSMORPHIC DISORDER; CHILD; CHROMOSOME DELETION; DEVELOPMENTAL DISORDER; EPILEPSY; FEMALE; HUMAN; INFANT; KARYOTYPE; LEARNING DISORDER; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; MICROARRAY ANALYSIS; MOTOR DYSFUNCTION; MUSCLE HYPOTONIA; PRESCHOOL CHILD; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SCHOOL CHILD;

EID: 78649231881     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2010.06.019     Document Type: Article
Times cited : (19)

References (13)
  • 1
    • 24944478689 scopus 로고    scopus 로고
    • Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH)
    • J. Schoumans, C. Ruivenkamp, E. Holmberg, M. Kyllerman, B.M. Anderlid, and M. Nordenskjold Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH) J Med Genet 42 2005 699 705
    • (2005) J Med Genet , vol.42 , pp. 699-705
    • Schoumans, J.1    Ruivenkamp, C.2    Holmberg, E.3    Kyllerman, M.4    Anderlid, B.M.5    Nordenskjold, M.6
  • 2
    • 58149153113 scopus 로고    scopus 로고
    • Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies
    • L. Edelmann, and K. Hirschhorn Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies Ann NY Acad Sci 1151 2009 157 166
    • (2009) Ann NY Acad Sci , vol.1151 , pp. 157-166
    • Edelmann, L.1    Hirschhorn, K.2
  • 3
    • 34548688666 scopus 로고    scopus 로고
    • Altered DNA copy number in patients with different seizure disorder type: By array-CGH
    • H.S. Kim, S.V. Yim, and K.H. Jung Altered DNA copy number in patients with different seizure disorder type: By array-CGH Brain Dev 29 2007 639 643
    • (2007) Brain Dev , vol.29 , pp. 639-643
    • Kim, H.S.1    Yim, S.V.2    Jung, K.H.3
  • 4
    • 25444445788 scopus 로고    scopus 로고
    • Gene expression profiling in neurological disorders: Toward a systems-level understanding of the brain
    • S.E. Baranzini Gene expression profiling in neurological disorders: Toward a systems-level understanding of the brain Neuromol Med 6 2004 31 51
    • (2004) Neuromol Med , vol.6 , pp. 31-51
    • Baranzini, S.E.1
  • 5
    • 0035205029 scopus 로고    scopus 로고
    • Blood genomic responses differ after stroke, seizures, hypoglycemia, and hypoxia: Blood genomic fingerprints of disease
    • Y. Tang, A. Lu, B.J. Aronow, and F.R. Sharp Blood genomic responses differ after stroke, seizures, hypoglycemia, and hypoxia: Blood genomic fingerprints of disease Ann Neurol 50 2001 699 707
    • (2001) Ann Neurol , vol.50 , pp. 699-707
    • Tang, Y.1    Lu, A.2    Aronow, B.J.3    Sharp, F.R.4
  • 6
    • 51449121623 scopus 로고    scopus 로고
    • Application of metaphase HR-CGH and targeted chromosomal microarray analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features
    • B. Nowakowska, P. Stankiewicz, and E. Obersztyn Application of metaphase HR-CGH and targeted chromosomal microarray analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features Am J Med Genet [A] 146A 2008 2361 2369
    • (2008) Am J Med Genet [A] , vol.146 , pp. 2361-2369
    • Nowakowska, B.1    Stankiewicz, P.2    Obersztyn, E.3
  • 7
    • 28644446258 scopus 로고    scopus 로고
    • American College of Medical Genetics guideline on the cytogenetic evaluation of the individual with developmental delay or mental retardation
    • L.G. Shaffer American College of Medical Genetics guideline on the cytogenetic evaluation of the individual with developmental delay or mental retardation Genet Med 7 2005 650 654
    • (2005) Genet Med , vol.7 , pp. 650-654
    • Shaffer, L.G.1
  • 8
    • 60449089258 scopus 로고    scopus 로고
    • Application of array-based comparative genome hybridization in children with developmental delay or mental retardation
    • J.S. Liang, K. Shimojima, and T. Yamamoto Application of array-based comparative genome hybridization in children with developmental delay or mental retardation Pediatr Neonatol 49 2008 213 217
    • (2008) Pediatr Neonatol , vol.49 , pp. 213-217
    • Liang, J.S.1    Shimojima, K.2    Yamamoto, T.3
  • 9
    • 43149107473 scopus 로고    scopus 로고
    • Medical genetics diagnostic evaluation of the child with global developmental delay or intellectual disability
    • J.B. Moeschler Medical genetics diagnostic evaluation of the child with global developmental delay or intellectual disability Curr Opin Neurol 21 2008 117 122
    • (2008) Curr Opin Neurol , vol.21 , pp. 117-122
    • Moeschler, J.B.1
  • 10
    • 31744437384 scopus 로고    scopus 로고
    • Determination of genomic breakpoints in an epileptic patient using genotyping array
    • T. Kojima, W. Mukai, and D. Fuma Determination of genomic breakpoints in an epileptic patient using genotyping array Biochem Biophys Res Commun 341 2006 792 796
    • (2006) Biochem Biophys Res Commun , vol.341 , pp. 792-796
    • Kojima, T.1    Mukai, W.2    Fuma, D.3
  • 11
    • 3042738883 scopus 로고    scopus 로고
    • Large-scale analysis of gene expression in epilepsy research: Is synthesis already possible?
    • K. Lukasiuk, and A. Pitkanen Large-scale analysis of gene expression in epilepsy research: Is synthesis already possible? Neurochem Res 29 2004 1169 1178
    • (2004) Neurochem Res , vol.29 , pp. 1169-1178
    • Lukasiuk, K.1    Pitkanen, A.2
  • 12
    • 0031608062 scopus 로고    scopus 로고
    • Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms
    • K. Mizugishi, K. Yamanaka, K. Kuwajima, and I. Kondo Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms J Hum Genet 43 1998 178 181
    • (1998) J Hum Genet , vol.43 , pp. 178-181
    • Mizugishi, K.1    Yamanaka, K.2    Kuwajima, K.3    Kondo, I.4
  • 13
    • 45749121948 scopus 로고    scopus 로고
    • Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: A validation of the practical performance of different array platforms
    • Z.F. Zhang, C. Ruivenkamp, and J. Staaf Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: A validation of the practical performance of different array platforms Eur J Hum Genet 16 2008 786 792
    • (2008) Eur J Hum Genet , vol.16 , pp. 786-792
    • Zhang, Z.F.1    Ruivenkamp, C.2    Staaf, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.