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New England Journal of Medicine
Volumn 351, Issue 8, 2004, Pages 822-824
Finding needles in haystacks - IRF6 gene variants in isolated cleft lip or cleft palate
Author keywords

[No Author keywords available]
Indexed keywords

CLEFT LIP; CLEFT PALATE; EDITORIAL; ENVIRONMENTAL EXPOSURE; GENE; GENE MUTATION; GENETIC RISK; GENETIC VARIABILITY; IRF6 GENE; PRIORITY JOURNAL;
EID: 4143060462     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJMe048164     Document Type: Editorial
Times cited : (8)
References (11)
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  • 3
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    • Erratum
    • van den Boogaard M-JH, Dorland M, Beemer FA, et al. MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat Genet 2000;24:342-3. [Erratum, Nat Genet 2000;25:125.]
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  • 4
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    • Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
    • Dode C, Levilliers J, Dupont J-M, et al. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. Nat Genet 2003;33:463-5.
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  • 5
    • 18644374446 scopus 로고    scopus 로고
    • Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
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    • Kondo, S.1    Schutte, B.C.2    Richardson, R.J.3
  • 6
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  • 7
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  • 8
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    • Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate
    • Zucchero TM, Cooper ME, Maher BS, et al. Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. N Engl J Med 2004;351:769-80.
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  • 9
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.