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Molecular Medicine Today
Volumn 6, Issue 1, 2000, Pages 12-
DiGeorge syndrome: Complex pathogenesis? Maybe, maybe not [2]
Author keywords

[No Author keywords available]
Indexed keywords

CHROMOSOME 22Q; DIGEORGE SYNDROME; EMBRYO DEVELOPMENT; HUMAN; INTERSTITIAL CHROMOSOME DELETION; LETTER; MOUSE; NONHUMAN; PHENOTYPE;
EID: 0033988353     PISSN: 13574310     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1357-4310(99)01627-5     Document Type: Letter
Times cited : (3)
References (6)
  • 1
    • 0033988564 scopus 로고    scopus 로고
    • Individual haploinsufficient loci and the complex phenotype of the DiGeorge syndrome
    • Novelli G.et al. Individual haploinsufficient loci and the complex phenotype of the DiGeorge syndrome. Mol. Med. Today. 6:2000;10-11.
    • (2000) Mol. Med. Today , vol.6 , pp. 10-11
    • Novelli, G.1
  • 2
    • 0016417459 scopus 로고
    • DiGeorge's or the III-IV pharyngeal pouch syndrome: Pathology and a theory of pathogenesis
    • Robinson H.B. Jr. DiGeorge's or the III-IV pharyngeal pouch syndrome: pathology and a theory of pathogenesis. Perspect. Pediatr. Pathol. 2:1975;173-206.
    • (1975) Perspect. Pediatr. Pathol. , vol.2 , pp. 173-206
    • Robinson H.B., Jr.1
  • 3
    • 0022520161 scopus 로고
    • Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor
    • Van Mierop L.H., Kutsche L.M. Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor. Am. J. Cardiol. 58:1986;133-137.
    • (1986) Am. J. Cardiol. , vol.58 , pp. 133-137
    • Van Mierop, L.H.1    Kutsche, L.M.2
  • 4
    • 0023075525 scopus 로고
    • The developmental field concept in pediatric pathology - especially with respect to fibular a/hypoplasia and the DiGeorge anomaly
    • Opitz J.M., Lewin S.O. The developmental field concept in pediatric pathology - especially with respect to fibular a/hypoplasia and the DiGeorge anomaly. Birth Defects Orig. Artic. Ser. 23:1987;277-292.
    • (1987) Birth Defects Orig. Artic. Ser. , vol.23 , pp. 277-292
    • Opitz, J.M.1    Lewin, S.O.2
  • 5
    • 0033582626 scopus 로고    scopus 로고
    • A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects
    • Yamagishi H.et al. A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects. Science. 283:1999;1158-1161.
    • (1999) Science , vol.283 , pp. 1158-1161
    • Yamagishi, H.1
  • 6
    • 0033598389 scopus 로고    scopus 로고
    • Congenital heart disease in mice deficient for the DiGeorge syndrome region
    • Lindsay E.A.et al. Congenital heart disease in mice deficient for the DiGeorge syndrome region. Nature. 401:1999;379-383.
    • (1999) Nature , vol.401 , pp. 379-383
    • Lindsay, E.A.1

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.