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Volumn 149, Issue 5, 2009, Pages 1033-1035

Late-onset lennox-gastaut syndrome in a patient with 15q11.2-q13.1 duplication

Author keywords

Autism; Chromosome disorders; DNA microarrays; Seizures

Indexed keywords

ADULT; ANAMNESIS; ARTICLE; CASE REPORT; CHROMOSOME 15Q; CHROMOSOME DUPLICATION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; HUMAN; LENNOX GASTAUT SYNDROME; PRIORITY JOURNAL;

EID: 66849101989     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32785     Document Type: Article
Times cited : (26)

References (9)
  • 2
    • 34247170891 scopus 로고    scopus 로고
    • 15q 11-13 GABA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders
    • Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM. 2007.15q 11-13 GABA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders. Hum Mol Genet 16:691-703.
    • (2007) Hum Mol Genet , vol.16 , pp. 691-703
    • Hogart, A.1    Nagarajan, R.P.2    Patzel, K.A.3    Yasui, D.H.4    Lasalle, J.M.5
  • 3
    • 64649098876 scopus 로고    scopus 로고
    • The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13
    • in press
    • Hogart A, Wu D, Lasalle JM, Schanen NC. 2008. The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13. Neurobiol Dis (in press).
    • (2008) Neurobiol Dis
    • Hogart, A.1    Wu, D.2    Lasalle, J.M.3    Schanen, N.C.4
  • 5
    • 3543038182 scopus 로고    scopus 로고
    • Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: Another mechanism for partial hexasomy
    • Mann SM, Wang NJ, Liu DH, Wang L, Schultz RA, Dorrani N, Sigman M, Schanen NC. 2004. Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: another mechanism for partial hexasomy. Hum Genet 115:104-111.
    • (2004) Hum Genet , vol.115 , pp. 104-111
    • Mann, S.M.1    Wang, N.J.2    Liu, D.H.3    Wang, L.4    Schultz, R.A.5    Dorrani, N.6    Sigman, M.7    Schanen, N.C.8
  • 8
    • 1842526843 scopus 로고    scopus 로고
    • Implication of human genome architecture for rearrangment-based disorders: The genome basis of disease
    • Shaw CJ, Lupski JR. 2004. Implication of human genome architecture for rearrangment-based disorders: the genome basis of disease. Hum Mol Genet 13:R57-R64.
    • (2004) Hum Mol Genet , vol.13
    • Shaw, C.J.1    Lupski, J.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.