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Journal Abstract Search

107 related items for PubMed ID: 16773506

  • 1. Neuroimaging in nine patients with inversion duplication of the short arm of chromosome 8.
    Feenstra I, van Ravenswaaij CM, van der Knaap MS, Willemsen MA.
    Neuropediatrics; 2006 Apr; 37(2):83-7. PubMed ID: 16773506
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  • 2. Agenesis of corpus callosum: clinical description and etiology.
    Marszał E, Jamroz E, Pilch J, Kluczewska E, Jabłecka-Deja H, Krawczyk R.
    J Child Neurol; 2000 Jun; 15(6):401-5. PubMed ID: 10868784
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  • 4. Large national series of patients with Xq28 duplication involving MECP2: Delineation of brain MRI abnormalities in 30 affected patients.
    El Chehadeh S, Faivre L, Mosca-Boidron AL, Malan V, Amiel J, Nizon M, Touraine R, Prieur F, Pasquier L, Callier P, Lefebvre M, Marle N, Dubourg C, Julia S, Sarret C, Francannet C, Laffargue F, Boespflug-Tanguy O, David A, Isidor B, Le Caignec C, Vigneron J, Leheup B, Lambert L, Philippe C, Cuisset JM, Andrieux J, Plessis G, Toutain A, Goldenberg A, Cormier-Daire V, Rio M, Bonnefont JP, Thevenon J, Echenne B, Journel H, Afenjar A, Burglen L, Bienvenu T, Addor MC, Lebon S, Martinet D, Baumann C, Perrin L, Drunat S, Jouk PS, Devillard F, Coutton C, Lacombe D, Delrue MA, Philip N, Moncla A, Badens C, Perreton N, Masurel A, Thauvin-Robinet C, Des Portes V, Guibaud L.
    Am J Med Genet A; 2016 Jan; 170A(1):116-29. PubMed ID: 26420639
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  • 5. Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.
    Sireteanu A, Braha E, Popescu R, Gramescu M, Gorduza EV, Rusu C.
    Rev Med Chir Soc Med Nat Iasi; 2013 Jan; 117(3):731-4. PubMed ID: 24502041
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  • 7. Familial white matter hypoplasia, agenesis of the corpus callosum, mental retardation and growth deficiency: a new distinctive syndrome.
    Curatolo P, Cilio MR, Del Giudice E, Romano A, Gaggero R, Pessagno A.
    Neuropediatrics; 1993 Apr; 24(2):77-82. PubMed ID: 8327066
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  • 8. Neuroimaging in mental retardation.
    Pandey A, Phadke SR, Gupta N, Phadke RV.
    Indian J Pediatr; 2004 Mar; 71(3):203-9. PubMed ID: 15080405
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  • 9. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
    Guo WJ, Callif-Daley F, Zapata MC, Miller ME.
    Am J Med Genet; 1995 Sep 11; 58(3):230-6. PubMed ID: 8533823
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  • 10. [Agenesis of the corpus callosum and epilepsy. 26 cases].
    Septien L, Gras P, Giroud M, Martin D, Binnert D, Dumas R.
    Rev Neurol (Paris); 1993 Sep 11; 149(4):257-61. PubMed ID: 8235222
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  • 12. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
    de Die-Smulders CE, Engelen JJ, Schrander-Stumpel CT, Govaerts LC, de Vries B, Vles JS, Wagemans A, Schijns-Fleuren S, Gillessen-Kaesbach G, Fryns JP.
    Am J Med Genet; 1995 Nov 20; 59(3):369-74. PubMed ID: 8599364
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  • 13. Hippocampal abnormalities in magnetic resonance imaging (MRI) of 15q duplication syndromes.
    Boronat S, Mehan WA, Shaaya EA, Thibert RL, Caruso P.
    J Child Neurol; 2015 Mar 20; 30(3):333-8. PubMed ID: 24985752
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  • 15. [Inverted duplication of the short arm of chromosome 8].
    Rodríguez Martínez L, Jiménez Muñoz-Delgado N, Nieto C, Martínez Carrascal A, López Grondona F, Martínez Frías ML.
    An Esp Pediatr; 2001 Nov 20; 55(5):458-62. PubMed ID: 11696311
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  • 16. Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.
    Barber JC, James RS, Patch C, Temple IK.
    Am J Med Genet; 1994 Apr 15; 50(3):296-9. PubMed ID: 8042676
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  • 18. MR imaging of periventricular leukomalacia in childhood.
    Flodmark O, Lupton B, Li D, Stimac GK, Roland EH, Hill A, Whitfield MF, Norman MG.
    AJR Am J Roentgenol; 1989 Mar 15; 152(3):583-90. PubMed ID: 2783813
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  • 20. Agenesis of the corpus callosum: clinical, neuroradiological and cytogenetic studies.
    Serur D, Jeret JS, Wisniewski K.
    Neuropediatrics; 1988 May 15; 19(2):87-91. PubMed ID: 2453812
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