메뉴 건너뛰기




Volumn 9, Issue 1, 1998, Pages 83-87

The feet in Pfeiffer's syndrome

Author keywords

Acrocephalosyndactyly; Craniosynostosis; Feet; Pfeiffer's's syndrome

Indexed keywords

ACROCEPHALOSYNDACTYLY; ARTICLE; BONE DYSPLASIA; CLINICAL ARTICLE; DISEASE SEVERITY; FEMALE; FOOT MALFORMATION; HALLUX; HUMAN; MALE; METATARSAL BONE; PHALANX; PRIORITY JOURNAL; PROSPECTIVE STUDY; RADIODIAGNOSIS; TARSAL BONE;

EID: 0031975801     PISSN: 10492275     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001665-199801000-00018     Document Type: Article
Times cited : (13)

References (17)
  • 1
    • 0000008683 scopus 로고
    • Dominant erbliche Akrocephalosyndaktylie
    • Pfeiffer RA. Dominant erbliche Akrocephalosyndaktylie. Z Kinderheilkd 1964;90:301-320
    • (1964) Z Kinderheilkd , vol.90 , pp. 301-320
    • Pfeiffer, R.A.1
  • 5
    • 0028046606 scopus 로고
    • A common mutation in the fibroblast growth factor receptor gene in Pfeiffer syndrome
    • Muenke M, Schell U, Hehr A, et al. A common mutation in the fibroblast growth factor receptor gene in Pfeiffer syndrome. Nat Genet 1994;8:269-274
    • (1994) Nat Genet , vol.8 , pp. 269-274
    • Muenke, M.1    Schell, U.2    Hehr, A.3
  • 6
    • 0029109137 scopus 로고
    • Identical mutations cause both both Pfeiffer and Crouzon syndrome phenotypes
    • Rutland P, Pulleyn LJ, Reardon W; et al. Identical mutations cause both both Pfeiffer and Crouzon syndrome phenotypes, Nat Genet 1995;9:173-176
    • (1995) Nat Genet , vol.9 , pp. 173-176
    • Rutland, P.1    Pulleyn, L.J.2    Reardon, W.3
  • 7
    • 0028798546 scopus 로고
    • Apert syndrome results from localised mutations of FGFR2 and is allelic with Crouzon syndrome
    • Wilkie AOM, Slaney SF, Oldridge M, et al. Apert syndrome results from localised mutations of FGFR2 and is allelic with Crouzon syndrome. Nat Genet 1995;9:165-172
    • (1995) Nat Genet , vol.9 , pp. 165-172
    • Wilkie, A.O.M.1    Slaney, S.F.2    Oldridge, M.3
  • 8
    • 0028113931 scopus 로고
    • Jackson-Weiss and Crouzon syndromes are allelic with mutations in the fibroblastic growth factor type 2
    • Jabs EW, Scott AF, Meyers G, et al. Jackson-Weiss and Crouzon syndromes are allelic with mutations in the fibroblastic growth factor type 2. Nat Genet 1994;8:275-279
    • (1994) Nat Genet , vol.8 , pp. 275-279
    • Jabs, E.W.1    Scott, A.F.2    Meyers, G.3
  • 9
    • 0027981524 scopus 로고
    • Mutations in the fibroblastic growth factor type 2 gene causes Crouzon syndrome
    • Reardon W, Winter RM, Rutland P, et al. Mutations in the fibroblastic growth factor type 2 gene causes Crouzon syndrome. Nat Genet 1994;8:98-103
    • (1994) Nat Genet , vol.8 , pp. 98-103
    • Reardon, W.1    Winter, R.M.2    Rutland, P.3
  • 10
    • 0013911559 scopus 로고
    • Progressive synostosis in Apert syndrome, with a description of the roengenographic changes in the feet
    • Schuerte EW, St Aubin PM. Progressive synostosis in Apert syndrome, with a description of the roengenographic changes in the feet. AJR Am J Roentgenol 1966;97:67-73
    • (1966) AJR Am J Roentgenol , vol.97 , pp. 67-73
    • Schuerte, E.W.1    St Aubin, P.M.2
  • 11
    • 84886621421 scopus 로고
    • Craniosynostosis, midface hypoplasia, and foot abnormalities: An autosomal dominant phenotype in a large Amish kindred
    • Jackson CE, Weiss L, Reynolds WA, et al. Craniosynostosis, midface hypoplasia, and foot abnormalities: an autosomal dominant phenotype in a large Amish kindred. J Pediatr 1976; 88:963-968
    • (1976) J Pediatr , vol.88 , pp. 963-968
    • Jackson, C.E.1    Weiss, L.2    Reynolds, W.A.3
  • 13
    • 0030743301 scopus 로고    scopus 로고
    • Anomalies of the hands in Pfeiffer syndrome and their clinical significance
    • Anderson PJ, Hall CM, Smith PJ, et al. Anomalies of the hands in Pfeiffer syndrome and their clinical significance. J Hand Surg 1997;22:537-540
    • (1997) J Hand Surg , vol.22 , pp. 537-540
    • Anderson, P.J.1    Hall, C.M.2    Smith, P.J.3
  • 14
    • 0027476349 scopus 로고
    • Pfeiffer syndrome update, clinical subtypes and guidelines for the differential diagnosis
    • Cohen MM. Pfeiffer syndrome update, clinical subtypes and guidelines for the differential diagnosis. Am J Med Genet 1993;45:300-307
    • (1993) Am J Med Genet , vol.45 , pp. 300-307
    • Cohen, M.M.1
  • 17
    • 0017717146 scopus 로고
    • Calcaneocuboid coalition in Crou-zon's syndrome (craniofacial dysostosis)
    • Craig CL, Goldberg MJ. Calcaneocuboid coalition in Crou-zon's syndrome (craniofacial dysostosis). J Bone Joint Surg 1977;59-A:826-827
    • (1977) J Bone Joint Surg , vol.59 A , pp. 826-827
    • Craig, C.L.1    Goldberg, M.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.