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152 related items for PubMed ID: 9151630

  • 1. Local, hypoplastic type of amelogenesis imperfecta: a clinical, genetic, radiological and dermatoglyphic study.
    Atasu M, Genc A, Namdar F.
    J Clin Pediatr Dent; 1996; 20(4):337-42. PubMed ID: 9151630
    [Abstract] [Full Text] [Related]

  • 2. Hypomaturation amelogenesis imperfecta: account of a family with an X-linked inheritance pattern.
    Bundzman ER, Modesto A.
    Braz Dent J; 1999; 10(2):111-6. PubMed ID: 10863398
    [Abstract] [Full Text] [Related]

  • 3. Congenital hypodontia of maxillary lateral incisors in association with coloboma of the iris and hypomaturation type of amelogenesis imperfecta in a large kindred.
    Atasu M, Eryilmaz A, Genc A, Ozcan M, Ozbayrak S.
    J Clin Pediatr Dent; 1997; 21(4):341-55. PubMed ID: 9484124
    [Abstract] [Full Text] [Related]

  • 4. The effects of acid-etching on enamel from different clinical variants of amelogenesis imperfecta: an SEM study.
    Seow WK, Amaratunge A.
    Pediatr Dent; 1998; 20(1):37-42. PubMed ID: 9524971
    [Abstract] [Full Text] [Related]

  • 5. [A familial strain of amelogenesis imperfecta hypoplastic type with dominant x-linked heredity].
    Cassese M, Grulliero A, Di Napoli G, Ventruto V.
    Minerva Stomatol; 1976; 25(2):89-94. PubMed ID: 1069908
    [Abstract] [Full Text] [Related]

  • 6. Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI).
    Masuya H, Shimizu K, Sezutsu H, Sakuraba Y, Nagano J, Shimizu A, Fujimoto N, Kawai A, Miura I, Kaneda H, Kobayashi K, Ishijima J, Maeda T, Gondo Y, Noda T, Wakana S, Shiroishi T.
    Hum Mol Genet; 2005 Mar 01; 14(5):575-83. PubMed ID: 15649948
    [Abstract] [Full Text] [Related]

  • 7. Hypocalcification type amelogenesis imperfecta in permanent dentition in association with heavily worn primary teeth, gingival hyperplasia, hypodontia and impacted teeth.
    Atasu M, Biren S, Mumcu G.
    J Clin Pediatr Dent; 1999 Mar 01; 23(2):117-21. PubMed ID: 10204452
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 47(2):148-56. PubMed ID: 284277
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 52(5):503-6. PubMed ID: 17316551
    [Abstract] [Full Text] [Related]

  • 10. Dental structural diseases mapping to human chromosome 4q21.
    MacDougall M.
    Connect Tissue Res; 2003 May 01; 44 Suppl 1():285-91. PubMed ID: 12952210
    [Abstract] [Full Text] [Related]

  • 11. Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q.
    Forsman K, Lind L, Bäckman B, Westermark E, Holmgren G.
    Hum Mol Genet; 1994 Sep 01; 3(9):1621-5. PubMed ID: 7833920
    [Abstract] [Full Text] [Related]

  • 12. Scanning electron microscopic study of hypoplastic type amelogenesis imperfecta in primary teeth.
    Uzamis M, Celik H, Erkmen N, Batirbaygil Y.
    J Clin Pediatr Dent; 1997 Sep 01; 21(3):265-8. PubMed ID: 9484138
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 64(2):111-4. PubMed ID: 16546853
    [Abstract] [Full Text] [Related]

  • 14. Amelogenesis imperfecta: local hypoplastic type with pulpal calcification.
    Gertzman GB, Gaston G, Quinn I.
    J Am Dent Assoc; 1979 Oct 01; 99(4):637-9. PubMed ID: 292722
    [Abstract] [Full Text] [Related]

  • 15. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
    Wright JT, Hart PS, Aldred MJ, Seow K, Crawford PJ, Hong SP, Gibson CW, Hart TC.
    Connect Tissue Res; 2003 Oct 01; 44 Suppl 1():72-8. PubMed ID: 12952177
    [Abstract] [Full Text] [Related]

  • 16. Amelogenesis imperfecta: a genetic study.
    Bäckman B, Holmgren G.
    Hum Hered; 1988 Oct 01; 38(4):189-206. PubMed ID: 3169793
    [Abstract] [Full Text] [Related]

  • 17. Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the X chromosome.
    Crawford PJ, Aldred MJ.
    Oral Surg Oral Med Oral Pathol; 1993 Aug 01; 76(2):187-91. PubMed ID: 8361730
    [Abstract] [Full Text] [Related]

  • 18. Craniofacial structure related to inheritance pattern in amelogenesis imperfecta.
    Bäckman B, Adolfsson U.
    Am J Orthod Dentofacial Orthop; 1994 Jun 01; 105(6):575-82. PubMed ID: 8198082
    [Abstract] [Full Text] [Related]

  • 19. [Amelogenesis imperfecta. Description of a clinical case].
    Villalobos S, Rivera H, Acevedo AM, Pinto-Cisternas J.
    Rev ADM; 1991 Jun 01; 48(2):95-100. PubMed ID: 1859812
    [Abstract] [Full Text] [Related]

  • 20. X-linked amelogenesis imperfecta. Presentation of two kindreds and a review of the literature.
    Crawford PJ, Aldred MJ.
    Oral Surg Oral Med Oral Pathol; 1992 Apr 01; 73(4):449-55. PubMed ID: 1574307
    [Abstract] [Full Text] [Related]

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