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Volumn 60, Issue 6, 2003, Pages 1033-1036

Periventricular heterotopia associated with chromosome 5p anomalies

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN REGION; CASE REPORT; CHROMOSOMAL LOCALIZATION; CHROMOSOME 5P; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; COMPLEX PARTIAL SEIZURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENETIC ASSOCIATION; GLIOSIS; HETEROTOPIA; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SCHOOL CHILD; TELOMERE; TRISOMY;

EID: 0037465847     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000052689.03214.61     Document Type: Article
Times cited : (91)

References (10)
  • 1
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    • Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia
    • Fox JW, Lamperti ED, Eksioglu YZ, et al. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia. Neuron 1998;21:1315-1325.
    • (1998) Neuron , vol.21 , pp. 1315-1325
    • Fox, J.W.1    Lamperti, E.D.2    Eksioglu, Y.Z.3
  • 2
    • 0035880455 scopus 로고    scopus 로고
    • Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females
    • Sheen VL, Dixon PH, Fox JW, et al. Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. Hum Mol Genet 2001;10:1775-1783.
    • (2001) Hum Mol Genet , vol.10 , pp. 1775-1783
    • Sheen, V.L.1    Dixon, P.H.2    Fox, J.W.3
  • 3
    • 0037177085 scopus 로고    scopus 로고
    • Familial periventricular heterotopia: Missense and distal truncating mutations of the FLN1 gene
    • Moro F, Carrozzo R, Veggiotti P, et al. Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene. Neurology 2002;58:916-921.
    • (2002) Neurology , vol.58 , pp. 916-921
    • Moro, F.1    Carrozzo, R.2    Veggiotti, P.3
  • 6
    • 0033736569 scopus 로고    scopus 로고
    • Periventricular nodular heterotopia in patients with filamin-1 gene mutations: Neuroimaging findings
    • Poussaint TY, Fox JW, Dobyns WB, et al. Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings. Pediatr Radiol 2000;30:748-755.
    • (2000) Pediatr Radiol , vol.30 , pp. 748-755
    • Poussaint, T.Y.1    Fox, J.W.2    Dobyns, W.B.3
  • 7
    • 0036556466 scopus 로고    scopus 로고
    • Identification of a dup(5)(p15.3) by multicolor banding
    • Riordan D, Vust A, Wickstrom D, et al. Identification of a dup(5)(p15.3) by multicolor banding. Clin Genet 2002;61:277-282.
    • (2002) Clin Genet , vol.61 , pp. 277-282
    • Riordan, D.1    Vust, A.2    Wickstrom, D.3
  • 8
    • 0037105012 scopus 로고    scopus 로고
    • De novo complete trisomy 5p: Clinical and neuroradiological findings
    • Grosso S, Cioni M, Garibaldi G, et al. De novo complete trisomy 5p: clinical and neuroradiological findings. Am J Med Genet 2002;112:56-60.
    • (2002) Am J Med Genet , vol.112 , pp. 56-60
    • Grosso, S.1    Cioni, M.2    Garibaldi, G.3
  • 9
    • 0032169814 scopus 로고    scopus 로고
    • Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies
    • Harrison KJ, Teshima IE, Silver MM, et al. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies. Am J Med Genet 1998;79:103-107.
    • (1998) Am J Med Genet , vol.79 , pp. 103-107
    • Harrison, K.J.1    Teshima, I.E.2    Silver, M.M.3
  • 10
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    • Beyond the Hox: How widespread is homeobox gene clustering?
    • Holland PW. Beyond the Hox: how widespread is homeobox gene clustering? J Anat 2001;199(pt 1-2):13-23.
    • (2001) J Anat , vol.199 , Issue.PART 1-2 , pp. 13-23
    • Holland, P.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.