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Journal Abstract Search

149 related items for PubMed ID: 197779

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  • 3. Congenital heart defects in oculodentodigital dysplasia: Report of two cases.
    Izumi K, Lippa AM, Wilkens A, Feret HA, McDonald-McGinn DM, Zackai EH.
    Am J Med Genet A; 2013 Dec; 161A(12):3150-4. PubMed ID: 24115525
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  • 4. The different appearance of the oculodentodigital dysplasia syndrome.
    Thomsen M, Schneider U, Weber M, Niethard FU.
    J Pediatr Orthop B; 1998 Jan; 7(1):23-6. PubMed ID: 9481652
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  • 5. [Oculodentodigital dysplasia: report of 2 familial cases].
    Camera G, Camera A, Pozzolo S, Costa M, Mantero R.
    Pathologica; 1994 Feb; 86(1):102-5. PubMed ID: 8072795
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  • 8. Oculodentodigital dysplasia.
    Doshi DC, Limdi PK, Parekh NV, Gohil NR.
    Indian J Ophthalmol; 2016 Mar; 64(3):227-30. PubMed ID: 27146935
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  • 10. Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature.
    Taşdelen E, Durmaz CD, Karabulut HG.
    Cytogenet Genome Res; 2018 Mar; 154(4):181-186. PubMed ID: 29902798
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  • 11. [Neurological presentations of oculodentodigital dysplasia].
    Rudenskaya GE, Dyomina NA, Bliznetz EA, Khlebnikova OV, Dadaly EL, Polyakov AV.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2018 Mar; 118(5):85-91. PubMed ID: 29927410
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  • 12. Dental management of oculodentodigital dysplasia: report of case.
    Dean JA, Jones JE, Vash BW.
    ASDC J Dent Child; 1986 Mar; 53(2):131-4. PubMed ID: 2937820
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  • 14. Generalised hypomineralisation of enamel in oculodentodigital dysplasia: comprehensive dental management of a case.
    Jensen ED.
    BMJ Case Rep; 2021 Jan 11; 14(1):. PubMed ID: 33431460
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  • 15. A novel GJA1 missense mutation in a Polish child with oculodentodigital dysplasia.
    Jamsheer A, Wisniewska M, Szpak A, Bugaj G, Krawczynski MR, Budny B, Wawrocka A, Latos-Bieleńska A.
    J Appl Genet; 2009 Jan 11; 50(3):297-9. PubMed ID: 19638688
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  • 16. Oculodentodigital dysplasia: disease spectrum in an eight-year-old boy, his parents and a sibling.
    Aminabadi NA, Ganji AT, Vafaei A, Pourkazemi M, Oskouei SG.
    J Clin Pediatr Dent; 2009 Jan 11; 33(4):337-41. PubMed ID: 19725242
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  • 17. The oculo-dento-digital syndrome: male-to-male transmission and variable expression in a family.
    Ioan DM, Dumitriu L, Belengeariu V, Fryns JP.
    Genet Couns; 1997 Jan 11; 8(2):87-90. PubMed ID: 9219005
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  • 18. A novel GJA1 mutation in oculodentodigital dysplasia with extensive loss of enamel.
    Porntaveetus T, Srichomthong C, Ohazama A, Suphapeetiporn K, Shotelersuk V.
    Oral Dis; 2017 Sep 11; 23(6):795-800. PubMed ID: 28258662
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  • 19. Evidence for genetic anticipation in the oculodentodigital syndrome.
    Shapiro RE, Griffin JW, Stine OC.
    Am J Med Genet; 1997 Jul 11; 71(1):36-41. PubMed ID: 9215766
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  • 20. Hallermann-Streiff syndrome: clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia?
    Spaepen A, Schrander-Stumpel C, Fryns JP, de Die-Smulders C, Borghgraef M, Van den Berghe H.
    Am J Med Genet; 1991 Dec 15; 41(4):517-20. PubMed ID: 1663704
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