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PUBMED FOR HANDHELDS

Journal Abstract Search


327 related items for PubMed ID: 4019732

  • 1.
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  • 2. Van der Woude syndrome: dentofacial features and implications for clinical practice.
    Lam AK, David DJ, Townsend GC, Anderson PJ.
    Aust Dent J; 2010 Mar; 55(1):51-8. PubMed ID: 20415912
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  • 3. Genetic epidemiology and control of genetic expression in van der Woude syndrome.
    Burdick AB.
    J Craniofac Genet Dev Biol Suppl; 1986 Mar; 2():99-105. PubMed ID: 3491128
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  • 4. [Van-der-Woude Syndrome].
    Del Frari B, Amort M, Janecke AR, Schutte BC, Piza-Katzer H.
    Klin Padiatr; 2008 Mar; 220(1):26-8. PubMed ID: 18095255
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  • 7. [Dominantly inherited lower lip fistulas and facial clefts (Van der Woude syndrome). A study of 52 cases].
    Kläusler M, Schinzel A, Gnoinski W, Hotz M, Perko M.
    Schweiz Med Wochenschr; 1987 Jan 24; 117(4):127-34. PubMed ID: 3823824
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  • 9. Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation.
    Beiraghi S, Miller-Chisholm A, Kimberling WJ, Sun CE, Wang YF, Russell LJ, Khoshnevisan M, Storm AL, Long RE, Witt PD, Mazaheri M, Diehl SR.
    J Craniofac Genet Dev Biol; 1999 Jan 24; 19(3):128-34. PubMed ID: 10589394
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  • 11. A novel mutation, 1234del(C), of the IRF6 in a Thai family with Van der Woude syndrome.
    Shotelersuk V, Srichomthong C, Yoshiura K, Niikawa N.
    Int J Mol Med; 2003 Apr 24; 11(4):505-7. PubMed ID: 12632105
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  • 12. Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.
    Item CB, Turhani D, Thurnher D, Yerit K, Sinko K, Wittwer G, Adeyemo WL, Frei K, Erginel-Unaltuna N, Watzinger F, Ewers R.
    Int J Mol Med; 2005 Feb 24; 15(2):247-51. PubMed ID: 15647839
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  • 14. Lower lip pits in a patient with van der Woude syndrome.
    Baghestani S, Sadeghi N, Yavarian M, Alghasi H.
    J Craniofac Surg; 2010 Sep 24; 21(5):1380-1. PubMed ID: 20818247
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  • 17. Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome.
    Scioletti AP, Brancati F, Gatta V, Antonucci I, Peissel B, Pizzuti A, Mortellaro C, Tetè S, Gherlone E, Palka G, Stuppia L.
    J Craniofac Surg; 2010 Sep 24; 21(5):1654-6. PubMed ID: 20856073
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  • 19. Identification of IRF6 gene variants in three families with Van der Woude syndrome.
    Tan EC, Lim EC, Yap SH, Lee ST, Cheng J, Por YC, Yeow V.
    Int J Mol Med; 2008 Jun 24; 21(6):747-51. PubMed ID: 18506368
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  • 20. The van der Woude syndrome in a large kindred: variability, penetrance, genetic risks.
    Janku P, Robinow M, Kelly T, Bralley R, Baynes A, Edgerton MT.
    Am J Med Genet; 1980 Jun 24; 5(2):117-23. PubMed ID: 7395906
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