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Volumn 42, Issue 1, 2005, Pages 54-57

An aetiological classification of birth defects for epidemiological research

Author keywords

[No Author keywords available]

Indexed keywords

ABORTIVE AGENT; ALCOHOL; ANTICONVULSIVE AGENT; COCAINE; CYTOTOXIC AGENT; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; FOLIC ACID ANTAGONIST; ILLICIT DRUG; LITHIUM; RETINOL DERIVATIVE; THALIDOMIDE; WARFARIN;

EID: 13244273746     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2004.023309     Document Type: Article
Times cited : (25)

References (15)
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  • 5
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    • Jones K, M Jones, J Fisher. A developmental approach to the classification of birth defects. Ann Plast Surg 1985;14:135-41.
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    • Jones, K.1    Jones, M.2    Fisher, J.3
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    • Chandley A. On the parental origin of de novo mutation in man. J Med Genet 1991;28:217-23.
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    • Chandley, A.1
  • 7
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    • Population surveillance of sentinal anomalies
    • Czeizel A. Population surveillance of sentinal anomalies. Mutat Res 1989;212:3-9.
    • (1989) Mutat Res , vol.212 , pp. 3-9
    • Czeizel, A.1
  • 10
    • 0029986964 scopus 로고    scopus 로고
    • A paternal wash in Apert syndrome
    • Sapienza C. A paternal wash in Apert syndrome. Nature Genet 1996;13:9-10.
    • (1996) Nature Genet , vol.13 , pp. 9-10
    • Sapienza, C.1
  • 11
    • 0042490798 scopus 로고    scopus 로고
    • Evidence for selective advantage of pathogenetic FGFR2 mutations in thèmale germ line
    • Goriely A, McVean GA, Rojmyr M, Ingemarsson B, Wilkie AO. Evidence for selective advantage of pathogenetic FGFR2 mutations in thèmale germ line. Science 2003;301:643-6.
    • (2003) Science , vol.301 , pp. 643-646
    • Goriely, A.1    McVean, G.A.2    Rojmyr, M.3    Ingemarsson, B.4    Wilkie, A.O.5
  • 13
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    • Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19
    • DeBaun M, Niemitz E, Feinberg A. Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19. Am J Hum Genet 2003;72:156-60.
    • (2003) Am J Hum Genet , vol.72 , pp. 156-160
    • DeBaun, M.1    Niemitz, E.2    Feinberg, A.3
  • 14
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    • Rare congenital disorders, imprinted genes, and assisted reproductive technology
    • Gosden R, Trasler J, Lucifero D, Faddy M. Rare congenital disorders, imprinted genes, and assisted reproductive technology. Lancet 2003;361:1975-7.
    • (2003) Lancet , vol.361 , pp. 1975-1977
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.