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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

262 related items for PubMed ID: 9484124

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  • 25. Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta.
    Gutierrez SJ, Chaves M, Torres DM, Briceño I.
    Arch Oral Biol; 2007 May; 52(5):503-6. PubMed ID: 17316551
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  • 26. Exclusion of p63 as a candidate gene for autosomal-dominant amelogenesis imperfecta.
    Gu X, Bäckman B, Coates PJ, Cullman I, Hellman U, Lind L, Nylander K.
    Acta Odontol Scand; 2006 Apr; 64(2):111-4. PubMed ID: 16546853
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  • 28. Autosomal recessive pigmented hypomaturation amelogenesis imperfecta. Report of a kindred.
    Witkop CJ, Kuhlmann W, Sauk J.
    Oral Surg Oral Med Oral Pathol; 1973 Sep; 36(3):367-82. PubMed ID: 4516465
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  • 29. New phenotype associated with an Arg116Cys mutation in the CRYAA gene: nuclear cataract, iris coloboma, and microphthalmia.
    Beby F, Commeaux C, Bozon M, Denis P, Edery P, Morlé L.
    Arch Ophthalmol; 2007 Feb; 125(2):213-6. PubMed ID: 17296897
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  • 30. Inherited dental anomalies: a review and prospects for the future role of clinicians.
    Pemberton TJ, Mendoza G, Gee J, Patel PI.
    J Calif Dent Assoc; 2007 May; 35(5):324-6, 328-33. PubMed ID: 17822158
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  • 31. Characteristics of incisor-premolar hypodontia in families.
    Arte S, Nieminen P, Apajalahti S, Haavikko K, Thesleff I, Pirinen S.
    J Dent Res; 2001 May; 80(5):1445-50. PubMed ID: 11437217
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  • 32. Familial aggregation of maxillary lateral incisor agenesis.
    Pinho T, Maciel P, Lemos C, Sousa A.
    J Dent Res; 2010 Jun; 89(6):621-5. PubMed ID: 20400722
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  • 34. Amelogenesis imperfecta among Israeli Jews and the description of a new type of local hypoplastic autosomal recessive amelogenesis imperfecta.
    Chosack A, Eidelman E, Wisotski I, Cohen T.
    Oral Surg Oral Med Oral Pathol; 1979 Feb; 47(2):148-56. PubMed ID: 284277
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  • 35. Kohlschütter-Tönz syndrome: epilepsy, dementia, and amelogenesis imperfecta.
    Zlotogora J, Fuks A, Borochowitz Z, Tal Y.
    Am J Med Genet; 1993 Jun 01; 46(4):453-4. PubMed ID: 8357021
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  • 37. Provisionally unique autosomal recessive chondrodysplasia punctata syndrome.
    Toriello HV, Higgins JV, Miller T.
    Am J Med Genet; 1993 Oct 01; 47(5):797-9. PubMed ID: 8267015
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  • 39. Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontism.
    Aldred MJ, Savarirayan R, Lamandé SR, Crawford PJ.
    Oral Dis; 2002 Jan 01; 8(1):62-8. PubMed ID: 11936459
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  • 40. Familial cases of missing mandibular incisor: three case presentations.
    Chai WL, Ngeow WC.
    Dent Update; 1999 Sep 01; 26(7):298-302. PubMed ID: 10765775
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