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Volumn 123, Issue 6, 2009, Pages 1811-1812

Discussion

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR TWIST; TRANSCRIPTION FACTOR TWIST1; UNCLASSIFIED DRUG; NUCLEAR PROTEIN; TWIST1 PROTEIN, HUMAN;

EID: 67649413386     PISSN: 00321052     EISSN: None     Source Type: Journal    
DOI: 10.1097/PRS.0b013e3181a3f213     Document Type: Note
Times cited : (4)

References (10)
  • 1
    • 0001636485 scopus 로고
    • Ein Beitrag zum Turmschaedelproblem (Pathogenese, Erblichkeit und Symptomatologie).
    • Saethre M. Ein Beitrag zum Turmschaedelproblem (Pathogenese, Erblichkeit und Symptomatologie). Dtsch Z Nervenheilkd. 1931;119:533-555.
    • (1931) Dtsch Z Nervenheilkd , vol.119 , pp. 533-555
    • Saethre, M.1
  • 2
    • 0001956946 scopus 로고
    • Eine eigenartige familiaere Entwicklungsstoerung (Akrocephalosyndaktylie, Dysostosis craniofacialis und Hypertelorismus)
    • Chotzen F. Eine eigenartige familiaere Entwicklungsstoerung (Akrocephalosyndaktylie, Dysostosis craniofacialis und Hypertelorismus). Monatsschr Kinderheilkd. 1932;55:97-122.
    • (1932) Monatsschr Kinderheilkd , vol.55 , pp. 97-122
    • Chotzen, F.1
  • 3
    • 0031012353 scopus 로고    scopus 로고
    • El Ghouzzi V,LeMerrerM,Perrin-Schmitt F, et al. Mutations of the TWIST gene in the Saethre-Chotzen syndrome. Nat Genet. 1997;15:42-46.
    • El Ghouzzi V,LeMerrerM,Perrin-Schmitt F, et al. Mutations of the TWIST gene in the Saethre-Chotzen syndrome. Nat Genet. 1997;15:42-46.
  • 4
    • 16944367030 scopus 로고    scopus 로고
    • A unique point mutation in the fibroblast growth factor 3 gene (FGFR3) defines a new craniosynostosis syndrome
    • Muenke M, Gripp KW, McDonald-McGinn DM, et al. A unique point mutation in the fibroblast growth factor 3 gene (FGFR3) defines a new craniosynostosis syndrome. Am J Hum Genet. 1997;60:555-564.
    • (1997) Am J Hum Genet , vol.60 , pp. 555-564
    • Muenke, M.1    Gripp, K.W.2    McDonald-McGinn, D.M.3
  • 6
    • 29644443643 scopus 로고    scopus 로고
    • Saethre-Chotzen syndrome caused by TWIST1 gene mutations: Functional differentiation from Muenke coronal synostosis syndrome
    • KressW,Schropp C,LiebG, etal. Saethre-Chotzen syndrome caused by TWIST1 gene mutations: Functional differentiation from Muenke coronal synostosis syndrome. Eur J Hum Genet. 2006;14:39-48.
    • (2006) Eur J Hum Genet , vol.14 , pp. 39-48
    • Kress, W.1    Schropp, C.2    Lieb, G.3
  • 7
    • 60549097195 scopus 로고    scopus 로고
    • Symptom outcomes following cranial vault expansion for craniosynostosis in children older than 2 years
    • discussion 298-299
    • Scott JR, Isom CN, Gruss JS, et al. Symptom outcomes following cranial vault expansion for craniosynostosis in children older than 2 years. Plast Reconstr Surg. 2009;123:289-297; discussion 298-299.
    • (2009) Plast Reconstr Surg , vol.123 , pp. 289-297
    • Scott, J.R.1    Isom, C.N.2    Gruss, J.S.3
  • 8
    • 0029883637 scopus 로고    scopus 로고
    • Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome
    • Slaney SF, Oldridge M, Hurst JA, et al. Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome. Am J Hum Genet. 1996;58:923-932.
    • (1996) Am J Hum Genet , vol.58 , pp. 923-932
    • Slaney, S.F.1    Oldridge, M.2    Hurst, J.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.