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Volumn 8, Issue 1, 1999, Pages 23-27

New syndromic entity of situs inversus totalis

Author keywords

Facio Cerebro Skeleto Cardiac syndrome; FCSCSI; MCA MR; Situs inversus totalis

Indexed keywords

ADULT; ARTICLE; BRACHYDACTYLY; BRAIN MALFORMATION; CASE REPORT; CONGENITAL HEART MALFORMATION; FACE DYSMORPHIA; FEMALE; HUMAN; MENTAL RETARDATION MALFORMATION SYNDROME; NUCLEAR MAGNETIC RESONANCE IMAGING; PES EQUINOVARUS; PRIORITY JOURNAL; QUADRIPLEGIA; RADIOGRAPHY; SHORT STATURE; SITUS INVERSUS;

EID: 0033044868     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199901000-00006     Document Type: Article
Times cited : (4)

References (7)
  • 1
    • 0025184104 scopus 로고
    • Clinical anophthalmia, dextrocardia, and skeletal anomalies in an infant born to consanguinous parents
    • Aughton DJ (1990). Clinical anophthalmia, dextrocardia, and skeletal anomalies in an infant born to consanguinous parents. Am J Med Genet 37:178-181.
    • (1990) Am J Med Genet , vol.37 , pp. 178-181
    • Aughton, D.J.1
  • 2
    • 0022537899 scopus 로고
    • Subclavian artery supply disruption sequence: Hypothesis of vascular actiology of Poland, Klipple-Feil and Moebius anomalies
    • Bowves-Bavinsck JNB, Weaver DD (1986). Subclavian artery supply disruption sequence: hypothesis of vascular actiology of Poland, Klipple-Feil and Moebius anomalies. Am J Med Genet 23:903-918.
    • (1986) Am J Med Genet , vol.23 , pp. 903-918
    • Bowves-Bavinsck, J.N.B.1    Weaver, D.D.2
  • 3
    • 0024854355 scopus 로고
    • Chondrodysplasia, situs inversus totalis, cleft epiglottis, and larynx, hexadactyly of hands and feet, pancreatic cystic dysplasia, renal dysplasia/absence, micropenis and ambiguous genitalia, imperforate anus
    • Frazier FC, Jequier S, Chen MF (1989). Chondrodysplasia, situs inversus totalis, eleft epiglottis, and larynx, hexadactyly of hands and feet, pancreatic cystic dysplasia, renal dysplasia/absence, micropenis and ambiguous genitalia, imperforate anus. Am J Med Genet 34:401-405.
    • (1989) Am J Med Genet , vol.34 , pp. 401-405
    • Frazier, F.C.1    Jequier, S.2    Chen, M.F.3
  • 6
    • 0024541976 scopus 로고
    • Growth hormone deficiency, wormian bones, dextrocardia, brachycamptodactyly, and other midline defects
    • Stratton, RF, Parker MW (1989). Growth hormone deficiency, wormian bones, dextrocardia, brachycamptodactyly, and other midline defects. Am J Med Genet 32:169-173.
    • (1989) Am J Med Genet , vol.32 , pp. 169-173
    • Stratton, R.F.1    Parker, M.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.