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Volumn 159, Issue 3, 2012, Pages 233-234

CHARGE syndrome - A rare combination of cardiac and endocrine disease

Author keywords

Cardiac genetics; Congenital heart disease; Endocrinology

Indexed keywords

FOLLITROPIN; LUTEINIZING HORMONE; TESTOSTERONE;

EID: 84865483460     PISSN: 01675273     EISSN: 18741754     Source Type: Journal    
DOI: 10.1016/j.ijcard.2012.05.104     Document Type: Article
Times cited : (2)

References (6)
  • 3
    • 79951805635 scopus 로고    scopus 로고
    • Role of rare cases in deciphering the mechanisms of congenital anomalies: CHARGE syndrome research
    • K. Kosaki Role of rare cases in deciphering the mechanisms of congenital anomalies: CHARGE syndrome research Congenital Anomalies 1 51 2011 12 15
    • (2011) Congenital Anomalies , vol.1 , Issue.51 , pp. 12-15
    • Kosaki, K.1
  • 4
    • 77649225132 scopus 로고    scopus 로고
    • Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome
    • G.E. Zentner, W.S. Layman, D.M. Martin, and P.C. Scacheri Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome Am J Med Genet A 3 152A 2010 674 686
    • (2010) Am J Med Genet A , vol.3 , Issue.152 A , pp. 674-686
    • Zentner, G.E.1    Layman, W.S.2    Martin, D.M.3    Scacheri, P.C.4
  • 6
    • 77956924029 scopus 로고    scopus 로고
    • Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome
    • K. Wessels, B. Bohnhorst, and I. Luhmer Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome European J Medical Genetics 5 53 2010 280 285
    • (2010) European J Medical Genetics , vol.5 , Issue.53 , pp. 280-285
    • Wessels, K.1    Bohnhorst, B.2    Luhmer, I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.