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Journal Abstract Search

165 related items for PubMed ID: 12131936

  • 1. Clinical, neuroimaging and cytogenetic findings in 20 patients with corpus callosum dysgenesis.
    dos Santos AC, Midleton SR, Fonseca RL, dos Santos SR, Llerena JC, Vargas FR.
    Arq Neuropsiquiatr; 2002 Jun; 60(2-B):382-5. PubMed ID: 12131936
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  • 2. [Associated brain anomalies and clinical findings in corpus callosum dysgenesis].
    Alkan A, Kutlu R, Baysal T, Siğirci A, Altinok T, Orkan I, Hallaç T, Saraç K.
    Tani Girisim Radyol; 2003 Dec; 9(4):411-7. PubMed ID: 14730948
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  • 3. Spectrum of corpus callosum agenesis.
    Sztriha L.
    Pediatr Neurol; 2005 Feb; 32(2):94-101. PubMed ID: 15664768
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  • 4. Corpus callosum agenesis in trisomy 8p11.23 and monosomy 4q34 because of maternal translocation.
    Işik U, Başaran S, Dehgan T, Apak M.
    Pediatr Neurol; 2008 Jul; 39(1):55-7. PubMed ID: 18555175
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  • 5. Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene.
    Caliebe A, Kroes HY, van der Smagt JJ, Martin-Subero JI, Tönnies H, van 't Slot R, Nievelstein RA, Muhle H, Stephani U, Alfke K, Stefanova I, Hellenbroich Y, Gillessen-Kaesbach G, Hochstenbach R, Siebert R, Poot M.
    Eur J Med Genet; 2010 Jul; 53(4):179-85. PubMed ID: 20382278
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  • 6. [Prognosis of isolated agenesis of the corpus callosum].
    Moutard ML, Lewin F, Baron JM, Kieffer V, Descamps P.
    Neurochirurgie; 1998 May; 44(1 Suppl):96-8. PubMed ID: 9757329
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  • 7. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA, Kamel AK, Ismail S, Helmy NA, Aglan MS, El Gammal M, El Ruby M, Mohamed AM.
    Genet Couns; 2007 May; 18(1):29-48. PubMed ID: 17515299
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  • 10. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
    Elia M, Striano P, Fichera M, Gaggero R, Castiglia L, Galesi O, Malacarne M, Pierluigi M, Amato C, Musumeci SA, Romano C, Majore S, Grammatico P, Zara F, Striano S, Faravelli F.
    Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
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  • 11. 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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  • 15. Unique mosaicism of tetraploidy and trisomy 8: clinical, cytogenetic, and molecular findings in a live-born infant.
    Roberts HE, Saxe DF, Muralidharan K, Coleman KB, Zacharias JF, Fernhoff PM.
    Am J Med Genet; 1996 Mar 29; 62(3):243-6. PubMed ID: 8882781
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  • 16. Agenesis of the corpus callosum. Its associated anomalies and syndromes with special reference to the Apert syndrome.
    Cohen MM, Kreiborg S.
    Neurosurg Clin N Am; 1991 Jul 29; 2(3):565-8. PubMed ID: 1821304
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  • 18. Mega-corpus callosum, polymicrogyria, and psychomotor retardation syndrome.
    Bindu PS, Taly AB, Sinha S, Bharath RD.
    Pediatr Neurol; 2010 Feb 29; 42(2):129-32. PubMed ID: 20117750
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  • 19. Agenesis of corpus callosum - a rare case.
    Desai AK, Bhide AG, Bhalerao SA.
    J Postgrad Med; 1999 Feb 29; 45(1):20-2. PubMed ID: 10734328
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  • 20. [Agenesis of the corpus callosum].
    Antonenko VG, Robak OP.
    Zh Vopr Neirokhir Im N N Burdenko; 1980 Feb 29; (4):59-60. PubMed ID: 7424326
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