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Volumn 27, Issue 3-4, 1996, Pages 150-155

Fibromatosis gingival, amelogénesis imperfecta, retardo en la erupción dental y retardo en el crecimiento y desarrollo. ¿Un nuevo síndrome?

Author keywords

[No Author keywords available]

Indexed keywords


EID: 45949109761     PISSN: 16579534     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (23)
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  • 8
    • 0016193707 scopus 로고
    • Variation in the inheritance and expression of gingival fibromatosis
    • Jorgenson RJ, Cocker ME. Variation in the inheritance and expression of gingival fibromatosis. J Periodontal 1974; 45: 472-77.
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    • Goldblatt, J.1    Singer, S.L.2
  • 11
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  • 15
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    • Rushton, M.A.1
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    • 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 PJM, Aldred MJ. Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the X chromosome. Oral Surg Oral Med Oral Pathol 1993; 76: 187-91.
    • (1993) Oral Surg Oral Med Oral Pathol , vol.76 , pp. 187-191
    • Crawford, P.J.M.1    Aldred, M.J.2
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  • 23
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    • Giansati JS, McKenzie WT, Owens FC. Gingival fibromatosis, hypertelorism, antimongoloid obliquity, multiple telangectasies and café-au-lait pigmentation: a unique combination of developmental anomalies. J Periodontol 1973; 44: 299-302.
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    • Giansati, J.S.1    McKenzie, W.T.2    Owens, F.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.