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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

236 related items for PubMed ID: 10029348

  • 41.
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  • 42. Contribution of magnetic resonance imaging in the evaluation of microcephaly.
    Steinlin M, Zürrer M, Martin E, Boesch C, Largo RH, Boltshauser E.
    Neuropediatrics; 1991 Nov; 22(4):184-9. PubMed ID: 1775213
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  • 45. Corpus callosum abnormalities and the controversy about the candidate genes located in 1q44.
    Orellana C, Roselló M, Monfort S, Oltra S, Quiroga R, Ferrer I, Martínez F.
    Cytogenet Genome Res; 2009 Nov; 127(1):5-8. PubMed ID: 20110648
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  • 50. Microcephaly thin corpus callosum intellectual disability syndrome caused by mutated TAF2.
    Hellman-Aharony S, Smirin-Yosef P, Halevy A, Pasmanik-Chor M, Yeheskel A, Har-Zahav A, Maya I, Straussberg R, Dahary D, Haviv A, Shohat M, Basel-Vanagaite L.
    Pediatr Neurol; 2013 Dec; 49(6):411-416.e1. PubMed ID: 24084144
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  • 52. [Ocular coloboma and results of brain MRI: preliminary results].
    Denis D, Girard N, Levy-Mozziconacci A, Berbis J, Matonti F.
    J Fr Ophtalmol; 2013 Mar; 36(3):210-20. PubMed ID: 23177150
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  • 53. Detecting 3D Corpus Callosum abnormalities in phenylketonuria.
    He Q, Christ SE, Karsch K, Moffitt AJ, Peck D, Duan Y.
    Int J Comput Biol Drug Des; 2009 Mar; 2(4):289-301. PubMed ID: 20090172
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  • 54. A case of Høyeraal-Hreidarsson syndrome: delayed myelination and hypoplasia of corpus callosum are other important signs.
    Akaboshi S, Yoshimura M, Hara T, Kageyama H, Nishikwa K, Kawakami T, Ieshima A, Takeshita K.
    Neuropediatrics; 2000 Jun; 31(3):141-4. PubMed ID: 10963101
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  • 55.
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  • 56. Cohen syndrome diagnosis using whole genome arrays.
    Rivera-Brugués N, Albrecht B, Wieczorek D, Schmidt H, Keller T, Göhring I, Ekici AB, Tzschach A, Garshasbi M, Franke K, Klopp N, Wichmann HE, Meitinger T, Strom TM, Hempel M.
    J Med Genet; 2011 Feb; 48(2):136-40. PubMed ID: 20921020
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  • 58. Neuroradiologic features of CASK mutations.
    Takanashi J, Arai H, Nabatame S, Hirai S, Hayashi S, Inazawa J, Okamoto N, Barkovich AJ.
    AJNR Am J Neuroradiol; 2010 Oct; 31(9):1619-22. PubMed ID: 20595373
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  • 59. Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination.
    Shimojima K, Okamoto N, Suzuki Y, Saito M, Mori M, Yamagata T, Momoi MY, Hattori H, Okano Y, Hisata K, Okumura A, Yamamoto T.
    J Hum Genet; 2012 Sep; 57(9):593-600. PubMed ID: 22718018
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  • 60.
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