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Volumn 24, Issue 3, 2003, Pages 394-397

Middle interhemispheric variant of holoprosencephaly associated with diffuse polymicrogyria

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN STEM; CASE REPORT; CLEFT PALATE; CLINICAL EXAMINATION; CLUBFOOT; DIAGNOSTIC IMAGING; DISEASE ASSOCIATION; HOLOPROSENCEPHALY; HUMAN; HYPOSPADIAS; INFANT; MALE; MICROGYRIA; MYOCLONUS SEIZURE; NUCLEAR MAGNETIC RESONANCE IMAGING;

EID: 0037344655     PISSN: 01956108     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (19)

References (15)
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  • 2
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    • The middle interhemispheric variant of holoprosencephaly
    • Simon EM, Hevner RF, Pinter JD, et al. The middle interhemispheric variant of holoprosencephaly. AJNR Am J Neuroradiol 2002;23:151-155
    • (2002) AJNR Am J Neuroradiol , vol.23 , pp. 151-155
    • Simon, E.M.1    Hevner, R.F.2    Pinter, J.D.3
  • 4
    • 0035311372 scopus 로고    scopus 로고
    • Holoprosencephaly due to mutation in ZIC2: Alanine tract expansion mutations may be caused by parental somatic recombination
    • Brown LY, Odent S, David V, et al. Holoprosencephaly due to mutation in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination. Hum Mol Genet 2001; 10:791-796
    • (2001) Hum Mol Genet , vol.10 , pp. 791-796
    • Brown, L.Y.1    Odent, S.2    David, V.3
  • 6
    • 0035067350 scopus 로고    scopus 로고
    • Cell migration and cerebral cortical development
    • Golden JA. Cell migration and cerebral cortical development. Neuropathol Appl Neurobiol 2001;27:22-28
    • (2001) Neuropathol Appl Neurobiol , vol.27 , pp. 22-28
    • Golden, J.A.1
  • 8
    • 18344389160 scopus 로고    scopus 로고
    • An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21
    • Piao X, Basel-Vanagaite L, Straussberg R, et al. An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21. Am J Hum Genet 2001;70:1028-1033
    • (2001) Am J Hum Genet , vol.70 , pp. 1028-1033
    • Piao, X.1    Basel-Vanagaite, L.2    Straussberg, R.3
  • 9
    • 0036201466 scopus 로고    scopus 로고
    • A locus for bilateral perisylvian polymicrogyria maps to Xq28
    • Villard L, Nguyen K, Cardoso C, et al. A locus for bilateral perisylvian polymicrogyria maps to Xq28. Am J Hum Genet 2001;70:1003-1008
    • (2001) Am J Hum Genet , vol.70 , pp. 1003-1008
    • Villard, L.1    Nguyen, K.2    Cardoso, C.3
  • 10
    • 0035570924 scopus 로고    scopus 로고
    • Neuropathologic research strategies in holoprosencephaly
    • Sarnat HB, Flores-Sarnat L. Neuropathologic research strategies in holoprosencephaly. J Child Neurol 2001;16:918-931
    • (2001) J Child Neurol , vol.16 , pp. 918-931
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  • 13
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    • Mediobasal and mantle defect of the prosencephalon: Lobar holoprosencephaly, schizencephaly and diabetes insipidus
    • Sztriha L, Varady E, Hetrtecant J, Nork M. Mediobasal and mantle defect of the prosencephalon: lobar holoprosencephaly, schizencephaly and diabetes insipidus. Neuropediatrics 1998;29:272-275
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    • Sztriha, L.1    Varady, E.2    Hetrtecant, J.3    Nork, M.4
  • 14
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    • Brunelli S, Faiella A, Carra V, et al. Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly. Nature Gen 1996;12:94-96
    • (1996) Nature Gen , vol.12 , pp. 94-96
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.