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Volumn 87, Issue 3, 1999, Pages 262-264

Two sisters with Toriello-Carey syndrome

Author keywords

Agenesis of the corpus callosum; Cardiac defect; Robin sequence; Telecanthus; Toriello Carey syndrome

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CONGENITAL HEART MALFORMATION; CORPUS CALLOSUM AGENESIS; CRANIOFACIAL MALFORMATION; EAR MALFORMATION; FEMALE; HUMAN; INFANT; MUSCLE HYPOTONIA; NOSE MALFORMATION; PRIORITY JOURNAL; TELECANTHUS;

EID: 0033607461     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19991126)87:3<262::AID-AJMG13>3.0.CO;2-3     Document Type: Article
Times cited : (13)

References (7)
  • 1
    • 0027203974 scopus 로고
    • Toriello-Carey syndrome: Report of a new case
    • Camera G, Righi E, Romagnoli G. 1993. Toriello-Carey syndrome: report of a new case. Clin Dysmorphol 2:260-263.
    • (1993) Clin Dysmorphol , vol.2 , pp. 260-263
    • Camera, G.1    Righi, E.2    Romagnoli, G.3
  • 2
    • 0029852706 scopus 로고    scopus 로고
    • Toriello-Carey syndrome: Evidence for X-linked inheritance
    • Czarnecki P, Lacombe D, Weiss L. 1996. Toriello-Carey syndrome: evidence for X-linked inheritance. Am J Med Genet 65:291-294.
    • (1996) Am J Med Genet , vol.65 , pp. 291-294
    • Czarnecki, P.1    Lacombe, D.2    Weiss, L.3
  • 3
    • 0026665913 scopus 로고
    • CNS midline anomalies in the Opitz G/BBB syndrome: Report on 12 Brazilian patients
    • Guion-Almeida ML, Richieri-Costa A. 1992. CNS midline anomalies in the Opitz G/BBB syndrome: report on 12 Brazilian patients. Am J Med Genet 43:918-928.
    • (1992) Am J Med Genet , vol.43 , pp. 918-928
    • Guion-Almeida, M.L.1    Richieri-Costa, A.2
  • 4
    • 0027249413 scopus 로고
    • Two siblings with midline defects and Hirschsprung disease: Variable expression of Toriello-Carey or new syndrome?
    • Jespers A, Buntinx I, Melis K, Vaerenberg M, Janssens G. 1993. Two siblings with midline defects and Hirschsprung disease: variable expression of Toriello-Carey or new syndrome? Am J Med Genet 47:299-302.
    • (1993) Am J Med Genet , vol.47 , pp. 299-302
    • Jespers, A.1    Buntinx, I.2    Melis, K.3    Vaerenberg, M.4    Janssens, G.5
  • 7
    • 0023693569 scopus 로고
    • Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: A new autosomal recessive syndrome?
    • Toriello HV, Carey JC. 1988. Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: a new autosomal recessive syndrome? Am J Med Genet 31:17-23.
    • (1988) Am J Med Genet , vol.31 , pp. 17-23
    • Toriello, H.V.1    Carey, J.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.