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Volumn 130, Issue 11, 2004, Pages 1298-1302

Tracheal anomalies in Pfeiffer syndrome

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR 2;

EID: 8844228845     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.130.11.1298     Document Type: Article
Times cited : (50)

References (10)
  • 1
    • 0000008683 scopus 로고
    • Dominant hereditary acrocephalosyndactylia
    • Pfeiffer RA. Dominant hereditary acrocephalosyndactylia [in German]. Z Kinderheik. 1964;90:301-320.
    • (1964) Z Kinderheik , vol.90 , pp. 301-320
    • Pfeiffer, R.A.1
  • 2
    • 0027476349 scopus 로고
    • Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis
    • Cohen MM. Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis. Am J Med Genet, 1993;45:300-307.
    • (1993) Am J Med Genet , vol.45 , pp. 300-307
    • Cohen, M.M.1
  • 3
    • 2742573684 scopus 로고
    • Letter to the editor: Reply to Dr Winter
    • Cohen MM, Barone CM. Letter to the editor: reply to Dr Winter. Am J Med Genet. 1994;49:358-359.
    • (1994) Am J Med Genet , vol.49 , pp. 358-359
    • Cohen, M.M.1    Barone, C.M.2
  • 4
    • 8844245896 scopus 로고    scopus 로고
    • Molecular characterization of Pfeiffer syndrome: Implications for prognosis and genetic counseling
    • Paper presented; November 8; Los Angeles, Calif, Abstract A253
    • McDonald-McGinn DM, DeBerardinis R, Bartlett S, et al. Molecular characterization of Pfeiffer syndrome: implications for prognosis and genetic counseling [abstract]. Paper presented at: Meeting of the American Society of Human Genetics; November 8, 2003; Los Angeles, Calif, Abstract A253.
    • (2003) Meeting of the American Society of Human Genetics
    • McDonald-McGinn, D.M.1    DeBerardinis, R.2    Bartlett, S.3
  • 5
    • 0032559241 scopus 로고    scopus 로고
    • Pfeiffer syndrome type 2: Further delineation and review of the literature
    • Plomp AS, Hamel BC, Cobben JM, et al. Pfeiffer syndrome type 2: further delineation and review of the literature. Am J Med Genet. 1998;75:245-251.
    • (1998) Am J Med Genet , vol.75 , pp. 245-251
    • Plomp, A.S.1    Hamel, B.C.2    Cobben, J.M.3
  • 6
    • 0031904629 scopus 로고
    • Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type III
    • Gripp KW, Stolle CA, McDonald-McGinn DM, et al. Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type III. Am J Med Genet. 1988;78:356-360.
    • (1988) Am J Med Genet , vol.78 , pp. 356-360
    • Gripp, K.W.1    Stolle, C.A.2    McDonald-McGinn, D.M.3
  • 8
    • 0028331964 scopus 로고
    • Congenital tracheal anomalies: Pathology study using serial macrosections and review of the literature
    • Chen LC, Holinger LD. Congenital tracheal anomalies: pathology study using serial macrosections and review of the literature. Pediatr Pathol. 1994;14:513-537.
    • (1994) Pediatr Pathol , vol.14 , pp. 513-537
    • Chen, L.C.1    Holinger, L.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.