메뉴 건너뛰기




Volumn 13, Issue 6, 2011, Pages 415-420

Clinical and genetic characterization of frontorhiny: Report of 3 novel cases and discussion of the surgical management

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84863260284     PISSN: 15212491     EISSN: 15383660     Source Type: Journal    
DOI: 10.1001/archfacial.2011.684     Document Type: Article
Times cited : (8)

References (11)
  • 1
    • 0023898135 scopus 로고
    • Frontonasal malformation as a field defect and in syndromic associations
    • Sedano HO, Gorlin RJ. Frontonasal malformation as a field defect and in syndromic associations. Oral Surg Oral Med Oral Pathol. 1988;65(6):704-710.
    • (1988) Oral Surg Oral Med Oral Pathol. , vol.65 , Issue.6 , pp. 704-710
    • Sedano, H.O.1    Gorlin, R.J.2
  • 2
    • 0014136944 scopus 로고
    • The median cleft face syndrome. Differential diagnosis of cranium bifidum occultum, hypertelorism, and median cleft nose, lip, and palate
    • DeMyer W. The median cleft face syndrome. Differential diagnosis of cranium bifidum occultum, hypertelorism, and median cleft nose, lip, and palate. Neurology. 1967;17(10):961-971.
    • (1967) Neurology , vol.17 , Issue.10 , pp. 961-971
    • DeMyer, W.1
  • 3
    • 0017161931 scopus 로고
    • Anatomical classifications of facial, cranio-facial and latero-facial clefts
    • Tessier P. Anatomical Classifications of Facial, Cranio-Facial and Latero-Facial Clefts. J Maxillofacial Surg. 1976;4:69-92.
    • (1976) J Maxillofacial Surg. , vol.4 , pp. 69-92
    • Tessier, P.1
  • 4
    • 0003442818 scopus 로고
    • Sadler T, ed. 6th ed. Baltimore: Williams and Wilkins
    • Sadler T. Langman's Medical Embryology. In: Sadler T, ed. 6th ed. Baltimore: Williams and Wilkins; 1990.
    • (1990) Langman's Medical Embryology
    • Sadler, T.1
  • 6
    • 65149104203 scopus 로고    scopus 로고
    • Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene
    • Twigg SR, Versnel SL, Nürnberg G, et al. Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. Am J Hum Genet. 2009;84(5):698-705.
    • (2009) Am J Hum Genet. , vol.84 , Issue.5 , pp. 698-705
    • Twigg, S.R.1    Versnel, S.L.2    Nürnberg, G.3
  • 7
  • 8
    • 48349117867 scopus 로고    scopus 로고
    • Rhinoplasty for African American patients: A retrospective review of 75 cases
    • Slupchynskyj O, Gieniusz M. Rhinoplasty for African American patients: a retrospective review of 75 cases. Arch Facial Plast Surg. 2008;10(4):232-236.
    • (2008) Arch Facial Plast Surg. , vol.10 , Issue.4 , pp. 232-236
    • Slupchynskyj, O.1    Gieniusz, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.