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Journal Abstract Search

121 related items for PubMed ID: 12124705

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  • 5. 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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  • 6. Diffusion-weighted magnetic resonance imaging of acute hypoxic-ischemic cerebral lesions in the survivor of a monochorionic twin pregnancy: case report.
    Righini A, Kustermann A, Parazzini C, Fogliani R, Ceriani F, Triulzi F.
    Ultrasound Obstet Gynecol; 2007 Apr; 29(4):453-6. PubMed ID: 17390325
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  • 7. Fetal intracranial haemorrhage and periventricular leukomalacia after second-trimester intrauterine fetal death in monochorionic twins.
    Ben Temime R, Chechia A, Attia L, Mrad M, Makhlouf T, Koubaa A.
    Tunis Med; 2008 Sep; 86(9):833-5. PubMed ID: 19472786
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  • 9. Reorganisation of the visual cortex in callosal agenesis and colpocephaly.
    Bittar RG, Ptito A, Dumoulin SO, Andermann F, Reutens DC.
    J Clin Neurosci; 2000 Jan; 7(1):13-5. PubMed ID: 10847643
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  • 14. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
    Chen CP, Lin SP, Chern SR, Lee CC, Huang JK, Wang W, Liao YW.
    Genet Couns; 2004 Jan; 15(4):437-42. PubMed ID: 15658619
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  • 16. Agenesis of the corpus callosum.
    Kelkar P, Lövblad KO, O'Callaghan B, Remonda L, Schroth G.
    JBR-BTR; 2000 Feb; 83(1):16. PubMed ID: 10769503
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  • 18. [Microcephaly and severe brain atrophy in a monochorionic twin pregnancy].
    Ferrer Lozano M, Gastón Faci A, Sánchez Andrés MT, Rebage Moisés V, Marco Tello A, López Pisón J.
    An Esp Pediatr; 1999 Apr; 50(4):405-7. PubMed ID: 10356837
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  • 20. Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family.
    Marafie MJ, Temtamy SA, Rajaram U, al-Awadi SA, el-Badramany MH, Farag TI.
    Am J Med Genet; 1996 Dec 18; 66(3):261-4. PubMed ID: 8985483
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