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Journal Abstract Search

262 related items for PubMed ID: 9484124

  • 1. 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]

  • 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
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  • 3. 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
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  • 4. 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; 23(2):117-21. PubMed ID: 10204452
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  • 7. [Familial occurrence of congenital aniridia].
    Zalewska R, Midro AT, Bakunowicz-Lazarczyk A, Proniewska-Skretek E.
    Klin Oczna; 1992; 94(5-6):159-60. PubMed ID: 1453680
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  • 8. New autosomal recessive multiple congenital abnormalities/mental retardation syndrome with craniofacial dysmorphism absent corpus callosum, iris colobomas and connective tissue dysplasia.
    Temtamy SA, Salam MA, Aboul-Ezz EH, Hussein HA, Helmy SA, Shalash BA.
    Clin Dysmorphol; 1996 Jul; 5(3):231-40. PubMed ID: 8818452
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  • 10. Midline facial defects with ocular colobomata.
    Temple IK, Brunner H, Jones B, Burn J, Baraitser M.
    Am J Med Genet; 1990 Sep; 37(1):23-7. PubMed ID: 1700608
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  • 12. Brief Clinical Report: coloboma hypospadias.
    Halal F, Farsky K.
    Am J Med Genet; 1981 Sep; 8(1):53-8. PubMed ID: 7246606
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  • 15. Exonal deletion of SLC24A4 causes hypomaturation amelogenesis imperfecta.
    Seymen F, Lee KE, Tran Le CG, Yildirim M, Gencay K, Lee ZH, Kim JW.
    J Dent Res; 2014 Apr; 93(4):366-70. PubMed ID: 24532815
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  • 17. Autosomal dominant typical coloboma associated with unilateral pseudoptosis, myopia and cataract.
    Porges Y.
    Cent Afr J Med; 1995 Aug; 41(8):255-7. PubMed ID: 7585914
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  • 18. Bilateral absence of maxillary and mandibular second premolars: a clinical, genetic and dermatoglyphic study.
    Atasu M, Akyüz S.
    J Clin Pediatr Dent; 1994 Aug; 18(3):219-21. PubMed ID: 8054309
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  • 19. Case reports of a new syndrome associating gingival fibromatosis and dental abnormalities in a consanguineous family.
    Martelli-Júnior H, Bonan PR, Dos Santos LA, Santos SM, Cavalcanti MG, Coletta RD.
    J Periodontol; 2008 Jul; 79(7):1287-96. PubMed ID: 18597613
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