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Volumn 118 A, Issue 1, 2003, Pages 86-89

Broad thumbs and halluces with deafness: A patient with Keipert syndrome

Author keywords

Abnormal epiphyses; Broad terminal phalanges; Deafness

Indexed keywords

ARTICLE; AUDIOLOGY; CASE REPORT; CLINICAL FEATURE; CONGENITAL MALFORMATION; FINGER MALFORMATION; HEARING IMPAIRMENT; HUMAN; KEIPERT SYNDROME; MALE; MUSCULOSKELETAL DISEASE; PRIORITY JOURNAL; RADIOGRAPHY; SCHOOL CHILD; SKELETON MALFORMATION;

EID: 0042822021     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.10063     Document Type: Article
Times cited : (10)

References (14)
  • 1
    • 0030457021 scopus 로고    scopus 로고
    • Keipert syndrome in two brothers from Turkey
    • Balci S, Dagli S. 1996. Keipert syndrome in two brothers from Turkey. Clin Genet 50:223-228.
    • (1996) Clin Genet , vol.50 , pp. 223-228
    • Balci, S.1    Dagli, S.2
  • 2
    • 0029798614 scopus 로고    scopus 로고
    • Identical mutations in three different fibroblast growth factor genes in autosomal dominant craniosynostosis syndromes
    • Bellus GA, Gaudenz K, Zackai EH, Clarke LA, Szabo J, Francomano CA, Muenke M. 1996. Identical mutations in three different fibroblast growth factor genes in autosomal dominant craniosynostosis syndromes. Nat Genet 14:174-176.
    • (1996) Nat Genet , vol.14 , pp. 174-176
    • Bellus, G.A.1    Gaudenz, K.2    Zackai, E.H.3    Clarke, L.A.4    Szabo, J.5    Francomano, C.A.6    Muenke, M.7
  • 3
    • 0033850732 scopus 로고    scopus 로고
    • Additional case of Keipert syndrome and review of the literature
    • Cappon SM, Khalifa MM. 2000. Additional case of Keipert syndrome and review of the literature. Med Sci Monit 6:776-778.
    • (2000) Med Sci Monit , vol.6 , pp. 776-778
    • Cappon, S.M.1    Khalifa, M.M.2
  • 4
    • 0041550795 scopus 로고
    • Genetic hearing loss associated with musculoskeletal disorders
    • Gorlin RJ, Toriello HV, Cohen MM Jr, editors. New York: Oxford University Press
    • Cohen MM Jr, Gorlin RJ. 1995. Genetic hearing loss associated with musculoskeletal disorders. In: Gorlin RJ, Toriello HV, Cohen MM Jr, editors. Hereditary hearing loss and its syndromes. New York: Oxford University Press. p 141-233.
    • (1995) Hereditary Hearing Loss and Its Syndromes , pp. 141-233
    • Cohen M.M., Jr.1    Gorlin, R.J.2
  • 9
    • 84993906223 scopus 로고
    • A new syndrome of broad terminal phalanges and facial abnormalities
    • Keipert JA, Fitzgerald MG, Danks DM. 1973. A new syndrome of broad terminal phalanges and facial abnormalities. Aust Paediatric J 9:10-13.
    • (1973) Aust Paediatric J , vol.9 , pp. 10-13
    • Keipert, J.A.1    Fitzgerald, M.G.2    Danks, D.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.