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Volumn 22, Issue 4, 1997, Pages 537-540

The hands in pfeiffer syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ACROCEPHALOSYNDACTYLY; ARTICLE; CHILD; CLINICAL ARTICLE; CRANIOFACIAL SYNOSTOSIS; DISTAL PHALANX; HAND FUNCTION; HAND MALFORMATION; HAND RADIOGRAPHY; HUMAN; HYPOPLASIA; INDEX FINGER; INFANT; MALE; OSTEOTOMY; PHALANX; THUMB; TOE;

EID: 0030743301     PISSN: 17531934     EISSN: 20436289     Source Type: Journal    
DOI: 10.1016/S0266-7681(97)80285-9     Document Type: Article
Times cited : (4)

References (14)
  • 3
    • 0001312459 scopus 로고
    • Syndromes with craniosynostosis
    • In MM Cohen (Ed.), New York: Raven Press
    • Cohen, MM (1986). Syndromes with craniosynostosis. In MM Cohen (Ed.), Cranio-synostosis diagnosis, evaluation and management (pp. 413-590). New York: Raven Press.
    • (1986) Cranio-Synostosis Diagnosis, Evaluation and Management , pp. 413-590
    • Cohen, M.M.1
  • 4
    • 0027476349 scopus 로고
    • Pfeiffer syndrome update, clinical subtypes and guidelines for the differential diagnosis
    • Cohen, MM (1993). Pfeiffer syndrome update, clinical subtypes and guidelines for the differential diagnosis. American Journal of Medical Genetics, 45, 300-307.
    • (1993) American Journal of Medical Genetics , vol.45 , pp. 300-307
    • Cohen, M.M.1
  • 5
    • 0017336111 scopus 로고
    • The acrocephalosyndactyly syndromes: A metacarpophalangeal pattern profile analysis
    • Escobar, V, and D Bixler (1977). The acrocephalosyndactyly syndromes: A metacarpophalangeal pattern profile analysis. Clinical Genetics, 11, 295-305.
    • (1977) Clinical Genetics , vol.11 , pp. 295-305
    • Escobar, V.1    Bixler, D.2
  • 7
    • 0019957742 scopus 로고
    • Pathological anatomy of the hands in Apert's syndrome
    • Green, SM (1982). Pathological anatomy of the hands in Apert's syndrome. Journal of Hand Surgery, 7, 450-453.
    • (1982) Journal of Hand Surgery , vol.7 , pp. 450-453
    • Green, S.M.1
  • 9
    • 0028046606 scopus 로고
    • A common mutation in the fibroblastic growth factor 1 gene in Pfeiffer syndrome
    • Muenke, M, U Schell, and A Hehr (1994). A common mutation in the fibroblastic growth factor 1 gene in Pfeiffer syndrome. Nature Genetics, 8, 269-274.
    • (1994) Nature Genetics , vol.8 , pp. 269-274
    • Muenke, M.1    Schell, U.2    Hehr, A.3
  • 10
    • 0000008683 scopus 로고
    • Dominant erbliche Akrocephalosyndaktylie
    • Pfeiffer, RA (1964). Dominant erbliche Akrocephalosyndaktylie. Kinderheilkunde, 90, 301-320.
    • (1964) Kinderheilkunde , vol.90 , pp. 301-320
    • Pfeiffer, R.A.1
  • 11
    • 2842580997 scopus 로고
    • Associated deformities of the head and hands
    • Pfeiffer, RA (1969). Associated deformities of the head and hands. Birth Defects, 5, 18-34.
    • (1969) Birth Defects , vol.5 , pp. 18-34
    • Pfeiffer, R.A.1
  • 13
    • 0028930046 scopus 로고
    • Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome
    • Schell, U, A Hehr, and GJ Feldman (1995). Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome. Human Molecular Genetics, 4, 323-328.
    • (1995) Human Molecular Genetics , vol.4 , pp. 323-328
    • Schell, U.1    Hehr, A.2    Feldman, G.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.