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Journal Abstract Search

151 related items for PubMed ID: 16371500

  • 1. Cerebellar hypoplasia and quadrupedal locomotion in humans as a recessive trait mapping to chromosome 17p.
    Türkmen S, Demirhan O, Hoffmann K, Diers A, Zimmer C, Sperling K, Mundlos S.
    J Med Genet; 2006 May; 43(5):461-4. PubMed ID: 16371500
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  • 5. "Unertan syndrome" in two Turkish families in relation to devolution and emergence of Homo erectus: neurological examination, MRI, and PET scans.
    Tan U, Pençe S, Yilmaz M, Ozkur A, Karaca S, Tan M, Karataş M.
    Int J Neurosci; 2008 Mar; 118(3):313-36. PubMed ID: 18300005
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  • 7. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
    Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA.
    Nat Genet; 2000 Sep; 26(1):93-6. PubMed ID: 10973257
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  • 8. X-linked nonprogressive congenital cerebellar hypoplasia: clinical description and mapping to chromosome Xq.
    Illarioshkin SN, Tanaka H, Markova ED, Nikolskaya NN, Ivanova-Smolenskaya IA, Tsuji S.
    Ann Neurol; 1996 Jul; 40(1):75-83. PubMed ID: 8687195
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  • 11. Lissencephaly and mild cerebellar vermis hypoplasia in a case of microcephaly and chorioretinal dysplasia.
    Lee BJ, Kim JH, Yu YS.
    Ophthalmic Genet; 2010 Jun; 31(2):89-93. PubMed ID: 20450312
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  • 13. Dominantly inherited hypoplasia of the vermis.
    Rivier F, Echenne B.
    Neuropediatrics; 1992 Aug; 23(4):206-8. PubMed ID: 1407388
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  • 14. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
    Pascual-Castroviejo I, Gutierrez M, Morales C, Gonzalez-Mediero I, Martínez-Bermejo A, Pascual-Pascual SI.
    Neuropediatrics; 1994 Aug; 25(4):183-90. PubMed ID: 7824090
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  • 16. Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11).
    Winner B, Uyanik G, Gross C, Lange M, Schulte-Mattler W, Schuierer G, Marienhagen J, Hehr U, Winkler J.
    Arch Neurol; 2004 Jan; 61(1):117-21. PubMed ID: 14732628
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  • 17. [Joubert's syndrome: report of 12 cases].
    Barreirinho MS, Teixeira J, Moreira NC, Bastos S, Gonçalvez S, Barbot MC.
    Rev Neurol; 2004 Jan; 32(9):812-7. PubMed ID: 11424029
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  • 19. [A new form of hereditary ataxia: X-linked congenital cerebellar hypoplasia (a clinical and molecular genetic analysis)].
    Illarioshkin SN, Ivanova-Smolenskaia IA, Markova ED, Nikol'skaia NN, Tsudzi S.
    Zh Nevrol Psikhiatr Im S S Korsakova; 1997 Jan; 97(10):17-23. PubMed ID: 9424342
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  • 20. Cerebellar dysgenesis and mental retardation associated with a complex chromosome rearrangement.
    Maserati E, Verri A, Seghezzi L, Tupler R, Federico A, Tiepolo L, Maraschio P.
    Ann Genet; 1999 Jan; 42(4):210-4. PubMed ID: 10674160
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