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Volumn 20, Issue 4, 2003, Pages 358-360

What syndrome is this?

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR 2;

EID: 0642314096     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1525-1470.2003.20419.x     Document Type: Article
Times cited : (6)

References (10)
  • 2
    • 0028012639 scopus 로고
    • Congenital craniofacial dysostosis and cutis gyratum: The Beare-Stevenson syndrome
    • Bratanic B, Praprotnik M, Novosel-Sever M. Congenital craniofacial dysostosis and cutis gyratum: the Beare-Stevenson syndrome. Eur J Pediatr 1994;153:184-186.
    • (1994) Eur J Pediatr , vol.153 , pp. 184-186
    • Bratanic, B.1    Praprotnik, M.2    Novosel-Sever, M.3
  • 4
    • 0016231276 scopus 로고
    • Cutis verticis gyrata and the Lennox syndrome
    • Paulson GW. Cutis verticis gyrata and the Lennox syndrome. Dev Med Child Neurol 1974;16:196-200.
    • (1974) Dev Med Child Neurol , vol.16 , pp. 196-200
    • Paulson, G.W.1
  • 5
    • 0024323235 scopus 로고
    • Association of cutis verticis gyrata with fragile X syndrome and fragility of chromosome 12
    • Schepis C, Palazzo R, Ragusa RM, Spina E, Barletta C. Association of cutis verticis gyrata with fragile X syndrome and fragility of chromosome 12 [letter]. Lancet 1989;2:279.
    • (1989) Lancet , vol.2 , pp. 279
    • Schepis, C.1    Palazzo, R.2    Ragusa, R.M.3    Spina, E.4    Barletta, C.5
  • 6
    • 0024957054 scopus 로고
    • Cutis verticis gyrata: A proposed classification
    • Rasmussen S, Frias J. Cutis verticis gyrata: a proposed classification. Dysmorph Clin Genet 1989;3:97-102.
    • (1989) Dysmorph Clin Genet , vol.3 , pp. 97-102
    • Rasmussen, S.1    Frias, J.2
  • 7
    • 0014499309 scopus 로고
    • Cutis gyratum, acanthosis nigricans and other congenital anomalies: A new syndrome
    • Beare JM, Dodge JA, Nevin NC. Cutis gyratum, acanthosis nigricans and other congenital anomalies: a new syndrome. Br J Dermatol 1969;81:241-247.
    • (1969) Br J Dermatol , vol.81 , pp. 241-247
    • Beare, J.M.1    Dodge, J.A.2    Nevin, N.C.3
  • 8
    • 0017979060 scopus 로고
    • Cutis gyratum and acanthosis nigricans with other congenital anomalies: A distinctive syndrome
    • Stevenson RE, Ferlauto GJ, Taylor HA. Cutis gyratum and acanthosis nigricans with other congenital anomalies: a distinctive syndrome. Am J Med Genet 1978;92:950-952.
    • (1978) Am J Med Genet , vol.92 , pp. 950-952
    • Stevenson, R.E.1    Ferlauto, G.J.2    Taylor, H.A.3
  • 9
    • 15844388219 scopus 로고    scopus 로고
    • Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome
    • Przylepa KA, Paznekas W, Zhang M, et al. Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome. Nat Genet 1996;13:492-494.
    • (1996) Nat Genet , vol.13 , pp. 492-494
    • Przylepa, K.A.1    Paznekas, W.2    Zhang, M.3
  • 10
    • 0033119157 scopus 로고    scopus 로고
    • Genomic organization of the human fibroblast growth factor receptor 2 (FGFR 2) gene and comparative analysis of the human FGFR gene family
    • Zhang Y, Gorry MC, Post JC, Ehrlich GD. Genomic organization of the human fibroblast growth factor receptor 2 (FGFR 2) gene and comparative analysis of the human FGFR gene family. Gene 1999;230:69-79.
    • (1999) Gene , vol.230 , pp. 69-79
    • Zhang, Y.1    Gorry, M.C.2    Post, J.C.3    Ehrlich, G.D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.