메뉴 건너뛰기




Volumn 80, Issue 5, 1998, Pages 459-465

Associated anomalies in individuals with polydactyly

Author keywords

13 trisomy; Meckel; Polydactyly; Polysyndactyly Down syndrome; Syndactyly

Indexed keywords

ARTICLE; CONGENITAL MALFORMATION; DISEASE ASSOCIATION; DOWN SYNDROME; HUMAN; MAJOR CLINICAL STUDY; MECKEL SYNDROME; POLYDACTYLY; PRIORITY JOURNAL; TRISOMY 13;

EID: 0032545315     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19981228)80:5<459::AID-AJMG5>3.0.CO;2-G     Document Type: Article
Times cited : (62)

References (17)
  • 7
    • 0015854442 scopus 로고
    • Polydactyly in Down's syndrome
    • Dignan PS (1973): Polydactyly in Down's syndrome. Am J Ment Défie 77: 486-491.
    • (1973) Am J Ment Défie , vol.77 , pp. 486-491
    • Dignan, P.S.1
  • 8
    • 9044223896 scopus 로고
    • Polydactylism of hand in southern Chinese
    • Handforth JR (1950): Polydactylism of hand in southern Chinese. Anat Rec 106:119-125.
    • (1950) Anat Rec , vol.106 , pp. 119-125
    • Handforth, J.R.1
  • 9
    • 0029974062 scopus 로고    scopus 로고
    • Major congenital malformations in Down syndrome
    • Källen B, Mastroiacovo P, Robert E (1996): Major congenital malformations in Down syndrome. Am J Med Genet 65:160-166.
    • (1996) Am J Med Genet , vol.65 , pp. 160-166
    • Källen, B.1    Mastroiacovo, P.2    Robert, E.3
  • 10
    • 0025185303 scopus 로고
    • On the measurement and interpretation of birth defect associations in epidemiologic studies
    • Khoury MJ, Levy WD, Erickson JD (1990): On the measurement and interpretation of birth defect associations in epidemiologic studies. Am J Med Genet 37:229-236.
    • (1990) Am J Med Genet , vol.37 , pp. 229-236
    • Khoury, M.J.1    Levy, W.D.2    Erickson, J.D.3
  • 11
    • 0016677913 scopus 로고
    • Hirschsprung's disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly in sibs: A case for fetoscopy
    • Laurence KM, Presser R, Rocker I, Pearson JF, Richard C (1975): Hirschsprung's disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly in sibs: a case for fetoscopy. J Med Genet 12:334-338.
    • (1975) J Med Genet , vol.12 , pp. 334-338
    • Laurence, K.M.1    Presser, R.2    Rocker, I.3    Pearson, J.F.4    Richard, C.5
  • 12
    • 33749779907 scopus 로고
    • Detection of Early Developmental Anomalies in Human Abortuses." Proceedings XIV International Congress of Pediatrics
    • Nishimura H (1974): "Detection Of Early Developmental Anomalies In Human Abortuses." Proceedings XIV International Congress of Pediatrics. Buenos Aires: Panamericana, p 159.
    • (1974) Buenos Aires: Panamericana, P , pp. 159
    • Nishimura, H.1
  • 13
    • 0028964780 scopus 로고
    • Segregation distortion in the offspring of Afroamerican fathers with postaxial polydactyly
    • Orioli IM (1995): Segregation distortion in the offspring of Afroamerican fathers with postaxial polydactyly. Am J Hum Genet 56:1207-1211.
    • (1995) Am J Hum Genet , vol.56 , pp. 1207-1211
    • Orioli, I.M.1
  • 14
    • 0030002181 scopus 로고    scopus 로고
    • The VACTERL association, epidemiologic definition and delineation
    • Rittler M, Paz JE, Castilla EE (1996): The VACTERL association, epidemiologic definition and delineation. Am J Med Genet 63:529-536.
    • (1996) Am J Med Genet , vol.63 , pp. 529-536
    • Rittler, M.1    Paz, J.E.2    Castilla, E.E.3
  • 15
    • 0030864277 scopus 로고    scopus 로고
    • VATERL: An epidemiologic analysis of risk factors
    • Rittler M, Paz JE, Castilla EE (1997): VATERL: an epidemiologic analysis of risk factors. Am J Med Genet 73:162-169.
    • (1997) Am J Med Genet , vol.73 , pp. 162-169
    • Rittler, M.1    Paz, J.E.2    Castilla, E.E.3
  • 16
    • 0027253535 scopus 로고
    • Fronto-nasal dysostosis, callosal agenesis, crossed-fused ectopia, tibial hemimelia, and preaxial polydactyly of feet-severe expression of the acrocallosal syndrome
    • Sueldo G, Fernandez MC (1993): Fronto-nasal dysostosis, callosal agenesis, crossed-fused ectopia, tibial hemimelia, and preaxial polydactyly of feet-severe expression of the acrocallosal syndrome. Am J Med Genet 46:355-357.
    • (1993) Am J Med Genet , vol.46 , pp. 355-357
    • Sueldo, G.1    Fernandez, M.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.