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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

262 related items for PubMed ID: 3605208

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  • 3. Otolaryngological manifestations of cleidocranial dysplasia, concentrating on audiological findings.
    Visosky AM, Johnson J, Bingea B, Gurney T, Lalwani AK.
    Laryngoscope; 2003 Sep; 113(9):1508-14. PubMed ID: 12972925
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  • 5. Apparent cleidocranial dysplasia associated with abnormalities of 8q22 in three individuals.
    Brueton LA, Reeve A, Ellis R, Husband P, Thompson EM, Kingston HM.
    Am J Med Genet; 1992 Jun 01; 43(3):612-8. PubMed ID: 1605259
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  • 7. RUNX2 mutations in cleidocranial dysplasia patients.
    Ryoo HM, Kang HY, Lee SK, Lee KE, Kim JW.
    Oral Dis; 2010 Jan 01; 16(1):55-60. PubMed ID: 19744171
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  • 10. Cleidocranial dysplasia in a mother and her daughter within the scope of neurosurgery. Report of two cases.
    Tokuc G, Boran P, Boran BO.
    J Neurosurg; 2006 Apr 01; 104(4 Suppl):290-2. PubMed ID: 16619644
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  • 12. [Pierre Marie-Sainton cleidocranial dysplasia].
    Diaconescu S, Păduraru G, Vâscu AM, Burlea M.
    Rev Med Chir Soc Med Nat Iasi; 2011 Apr 01; 115(2):341-8. PubMed ID: 21870721
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  • 14. Cleidocranial dysplasia: oral features and genetic analysis of 11 patients.
    Bufalino A, Paranaíba LM, Gouvêa AF, Gueiros LA, Martelli-Júnior H, Junior JJ, Lopes MA, Graner E, De Almeida OP, Vargas PA, Coletta RD.
    Oral Dis; 2012 Mar 01; 18(2):184-90. PubMed ID: 22023169
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  • 15. Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2 : possible involvement of non-genetic or epigenetic regulation.
    Suda N, Hamada T, Hattori M, Torii C, Kosaki K, Moriyama K.
    Orthod Craniofac Res; 2007 Nov 01; 10(4):222-5. PubMed ID: 17973689
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  • 16. Cleidocranial dysplasia: a case report.
    Karagüzel G, Aktürk FA, Okur E, Gümele HR, Gedik Y, Okten A.
    J Clin Res Pediatr Endocrinol; 2010 Nov 01; 2(3):134-6. PubMed ID: 21274329
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  • 18. Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 families.
    Dinçsoy Bir F, Dinçkan N, Güven Y, Baş F, Altunoğlu U, Kuvvetli SS, Poyrazoğlu Ş, Toksoy G, Kayserili H, Uyguner ZO.
    Eur J Med Genet; 2017 Mar 01; 60(3):163-168. PubMed ID: 28027977
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  • 19. Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literature.
    Fernandez BA, Siegel-Bartelt J, Herbrick JA, Teshima I, Scherer SW.
    Clin Genet; 2005 Oct 01; 68(4):349-59. PubMed ID: 16143022
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