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Volumn 30, Issue 3, 2012, Pages 258-261

Seckel syndrome: A report of a case

Author keywords

Bird headed dwarf; Mental retardation; Seckel syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHEILITIS; CHILD; DENTAL CARIES; DENTAL PROCEDURE; DWARFISM; FACIES; FEMALE; GINGIVITIS; HUMAN; INTELLECTUAL IMPAIRMENT; MALOCCLUSION; MICROCEPHALY; MOUTH DISEASE; PULPITIS; TOOTH DISEASE; TOOTH FRACTURE;

EID: 84872019974     PISSN: 09704388     EISSN: 19983905     Source Type: Journal    
DOI: 10.4103/0970-4388.105021     Document Type: Article
Times cited : (8)

References (10)
  • 1
    • 10644281262 scopus 로고    scopus 로고
    • Seckel cell syndromes or Seckel variants?
    • Cherian MP. Seckel cell syndromes or Seckel variants? Ann Saudi Med 2004;24: 469-72.
    • (2004) Ann Saudi Med , vol.24 , pp. 469-472
    • Cherian, M.P.1
  • 2
    • 9344239397 scopus 로고    scopus 로고
    • Seckel syndrome with polyarteritis nodosa
    • Kutlu R, Alkan A, Kutlu O, Yakinci C. Seckel syndrome with polyarteritis nodosa. Indian Pediatr 2004;41: 1158-61. (Pubitemid 39557087)
    • (2004) Indian Pediatrics , vol.41 , Issue.11 , pp. 1158-1161
    • Kutlu, R.1    Alkan, A.2    Kutlu, O.3    Yakinci, C.4
  • 3
    • 84872008044 scopus 로고    scopus 로고
    • Seckel syndrome
    • [August 2011]
    • Faivre L, Daire VC. Seckel syndrome. Orphanet Encyclopedia 2005. Available from: http://www.orpha.net/data/patho/GB/ UK-Seckel (05).pdf [August 2011]
    • (2005) Orphanet Encyclopedia
    • Faivre, L.1    Daire, V.C.2
  • 6
    • 65949107060 scopus 로고    scopus 로고
    • Prenatal diagnosis of Seckel Syndrome on 3-dimensional sonography and magnetic resonance imaging
    • Napolitano R, Maroutti GM, Quarantelli M, Martinelli P, Paladini D. Prenatal diagnosis of Seckel Syndrome on 3-dimensional sonography and magnetic resonance imaging. J Ultrasound Med 2009;28: 369-74.
    • (2009) J Ultrasound Med , vol.28 , pp. 369-374
    • Napolitano, R.1    Maroutti, G.M.2    Quarantelli, M.3    Martinelli, P.4    Paladini, D.5
  • 7
    • 0030881107 scopus 로고    scopus 로고
    • Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome
    • DOI 10.1002/(SICI)1096-8628(19970905)71:4<479::AID-AJMG21>3.0.CO;2- C
    • Courtens W, Speleman F, Messaian L, Bormans J, Van Roy N, Vamos E. Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome. Am J Med Genet 1997;71: 479-85. (Pubitemid 27371852)
    • (1997) American Journal of Medical Genetics , vol.71 , Issue.4 , pp. 479-485
    • Courtens, W.1    Speleman, F.2    Messiaen, L.3    Bormans, J.4    Van Roy, N.5    Vamos, E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.