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Journal Abstract Search

277 related items for PubMed ID: 11449490

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  • 23. New trends in neuronal migration disorders.
    Verrotti A, Spalice A, Ursitti F, Papetti L, Mariani R, Castronovo A, Mastrangelo M, Iannetti P.
    Eur J Paediatr Neurol; 2010 Jan; 14(1):1-12. PubMed ID: 19264520
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  • 30. Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis.
    Leventer RJ, Pilz DT, Matsumoto N, Ledbetter DH, Dobyns WB.
    Mol Med Today; 2000 Jul; 6(7):277-84. PubMed ID: 10859564
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  • 31. X-linked malformations of neuronal migration.
    Dobyns WB, Andermann E, Andermann F, Czapansky-Beilman D, Dubeau F, Dulac O, Guerrini R, Hirsch B, Ledbetter DH, Lee NS, Motte J, Pinard JM, Radtke RA, Ross ME, Tampieri D, Walsh CA, Truwit CL.
    Neurology; 1996 Aug; 47(2):331-9. PubMed ID: 8757001
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  • 32. A locus for bilateral perisylvian polymicrogyria maps to Xq28.
    Villard L, Nguyen K, Cardoso C, Martin CL, Weiss AM, Sifry-Platt M, Grix AW, Graham JM, Winter RM, Leventer RJ, Dobyns WB.
    Am J Hum Genet; 2002 Apr; 70(4):1003-8. PubMed ID: 11822025
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  • 34. Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.
    Sakamoto M, Ono J, Okada S, Nakamura Y, Kurahashi H.
    J Hum Genet; 2000 Apr; 45(3):167-70. PubMed ID: 10807542
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  • 37. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 38. Overlapping cortical malformations and mutations in TUBB2B and TUBA1A.
    Cushion TD, Dobyns WB, Mullins JG, Stoodley N, Chung SK, Fry AE, Hehr U, Gunny R, Aylsworth AS, Prabhakar P, Uyanik G, Rankin J, Rees MI, Pilz DT.
    Brain; 2013 Feb; 136(Pt 2):536-48. PubMed ID: 23361065
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  • 39. Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.
    Pinard JM, Motte J, Chiron C, Brian R, Andermann E, Dulac O.
    J Neurol Neurosurg Psychiatry; 1994 Aug; 57(8):914-20. PubMed ID: 8057113
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  • 40. [Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing].
    Bahi-Buisson N, Boddaert N, Saillour Y, Souville I, Poirier K, Léger PL, Castelnau L, Plouin P, Carion N, Beldjord C, Chelly J.
    Rev Neurol (Paris); 2008 Dec; 164(12):995-1009. PubMed ID: 18808783
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