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Volumn 70, Issue 2, 2003, Pages 177-179

Diagnosing acrocallosal syndrome

Author keywords

Acrocallosal syndrome (ACS); Agenesis of corpus callosum; Polydactyly

Indexed keywords

ACROCALLOSAL SYNDROME; AGE; ARTICLE; CASE REPORT; CLINICAL FEATURE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; GENETIC DISORDER; HUMAN; INFANT; MALE;

EID: 0037293447     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02723750     Document Type: Article
Times cited : (1)

References (7)
  • 3
    • 0024363204 scopus 로고
    • Acrocallosal syndrome: Additional manifestations
    • Casamassima AC, Beneck D, Gewitz MH et al. Acrocallosal syndrome: Additional manifestations. Am J Med Genet 1989; 32:311-317.
    • (1989) Am J Med Genet , vol.32 , pp. 311-317
    • Casamassima, A.C.1    Beneck, D.2    Gewitz, M.H.3
  • 5
    • 0025339284 scopus 로고
    • How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case
    • Turrolla L, Clementi M, Tenconi R. How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case. J Med Genet 1990; 27: 516-518.
    • (1990) J Med Genet , vol.27 , pp. 516-518
    • Turrolla, L.1    Clementi, M.2    Tenconi, R.3
  • 6
    • 0031047040 scopus 로고    scopus 로고
    • Acrocallosal syndrome in an Algerian boy born to consanguineous parents : Review of the literature and further delineation of the syndrome
    • Courtens W, Vamos E, Christophe C, Schinzel A. Acrocallosal syndrome in an Algerian boy born to consanguineous parents : review of the literature and further delineation of the syndrome. Am J Med Genet 1997; 69: 17-22.
    • (1997) Am J Med Genet , vol.69 , pp. 17-22
    • Courtens, W.1    Vamos, E.2    Christophe, C.3    Schinzel, A.4
  • 7
    • 0029931942 scopus 로고    scopus 로고
    • Clinical and molecualr cytogenetic observations in three cases of "Trisomy 12p syndrome"
    • Rauch A, Trautmann U, Pfeiffer RA. Clinical and molecualr cytogenetic observations in three cases of "Trisomy 12p syndrome". Am J Med Genet 1996; 63: 243-249.
    • (1996) Am J Med Genet , vol.63 , pp. 243-249
    • Rauch, A.1    Trautmann, U.2    Pfeiffer, R.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.