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134 related items for PubMed ID: 10894430

  • 1. Popliteal pterygium syndrome in a Swedish family--clinical findings and genetic analysis with the van der Woude syndrome locus at 1q32-q41.
    Wong FK, Gustafsson B.
    Acta Odontol Scand; 2000 Apr; 58(2):85-8. PubMed ID: 10894430
    [Abstract] [Full Text] [Related]

  • 2. Van der Woude and Popliteal Pterygium Syndromes: Broad intrafamilial variability in a three generation family with mutation in IRF6.
    Busche A, Hehr U, Sieg P, Gillessen-Kaesbach G.
    Am J Med Genet A; 2016 Sep; 170(9):2404-7. PubMed ID: 27286731
    [Abstract] [Full Text] [Related]

  • 3. Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.
    Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J.
    Eur J Hum Genet; 2001 Oct; 9(10):747-52. PubMed ID: 11781685
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  • 4. Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32.
    Lees MM, Winter RM, Malcolm S, Saal HM, Chitty L.
    J Med Genet; 1999 Dec; 36(12):888-92. PubMed ID: 10593995
    [Abstract] [Full Text] [Related]

  • 5. Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate.
    Pegelow M, Koillinen H, Magnusson M, Fransson I, Unneberg P, Kere J, Karsten A, Peyrard-Janvid M.
    Cleft Palate Craniofac J; 2014 Jan; 51(1):49-55. PubMed ID: 23394314
    [Abstract] [Full Text] [Related]

  • 6. Van der Woude and Popliteal Pterygium Syndromes.
    Bennun RD, Stefano E, Moggi LE.
    J Craniofac Surg; 2018 Sep; 29(6):1434-1436. PubMed ID: 29916977
    [Abstract] [Full Text] [Related]

  • 7. Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome.
    Sander A, Schmelzle R, Murray J.
    Hum Mol Genet; 1994 Apr; 3(4):575-8. PubMed ID: 8069301
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  • 8. A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.
    Schutte BC, Bjork BC, Coppage KB, Malik MI, Gregory SG, Scott DJ, Brentzell LM, Watanabe Y, Dixon MJ, Murray JC.
    Genome Res; 2000 Jan; 10(1):81-94. PubMed ID: 10645953
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  • 9. Clinical and genetic studies of Van der Woude syndrome in Sweden.
    Wong FK, Karsten A, Larson O, Huggare J, Hagberg C, Larsson C, Teh BT, Linder-Aronson S.
    Acta Odontol Scand; 1999 Apr; 57(2):72-6. PubMed ID: 10445358
    [Abstract] [Full Text] [Related]

  • 10. Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.
    Schutte BC, Basart AM, Watanabe Y, Laffin JJ, Coppage K, Bjork BC, Daack-Hirsch S, Patil S, Dixon MJ, Murray JC.
    Am J Med Genet; 1999 May 21; 84(2):145-50. PubMed ID: 10323740
    [Abstract] [Full Text] [Related]

  • 11. Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes.
    Leslie EJ, Mancuso JL, Schutte BC, Cooper ME, Durda KM, L'Heureux J, Zucchero TM, Marazita ML, Murray JC.
    Am J Med Genet A; 2013 Oct 21; 161A(10):2535-2544. PubMed ID: 23949966
    [Abstract] [Full Text] [Related]

  • 12. Anatomic Severity, Midfacial Growth, and Speech Outcomes in Van der Woude/Popliteal Pterygium Syndromes Compared to Nonsyndromic Cleft Lip/Palate.
    Reardon JB, Brustowicz KA, Marrinan EM, Mulliken JB, Padwa BL.
    Cleft Palate Craniofac J; 2015 Nov 21; 52(6):676-81. PubMed ID: 25210863
    [Abstract] [Full Text] [Related]

  • 13. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
    Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Arcos-Burgos M, Valencia C, Houdayer C, Bahuau M, Moretti-Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC.
    Nat Genet; 2002 Oct 21; 32(2):285-9. PubMed ID: 12219090
    [Abstract] [Full Text] [Related]

  • 14. Phenotypic variability in van der Woude syndrome.
    Lacombe D, Pedespan JM, Fontan D, Chateil JF, Verloes A.
    Genet Couns; 1995 Oct 21; 6(3):221-6. PubMed ID: 8588850
    [Abstract] [Full Text] [Related]

  • 15. Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family.
    Manjegowda DS, Prasad M, Veerappa AM, Ramachandra NB.
    Genet Res (Camb); 2014 Oct 10; 96():e12. PubMed ID: 25579819
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  • 17. Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414.
    Sander A, Murray JC, Scherpbier-Heddema T, Buetow KH, Weissenbach J, Zingg M, Ludwig K, Schmelzle R.
    Am J Hum Genet; 1995 Jan 10; 56(1):310-8. PubMed ID: 7825592
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  • 19. Novel Mutations in the IRF6 Gene on the Background of Known Polymorphisms in Polish Patients With Orofacial Clefting.
    Charzewska A, Obersztyn E, Hoffman-Zacharska D, Lenart J, Poznański J, Bal J.
    Cleft Palate Craniofac J; 2015 Sep 10; 52(5):e161-7. PubMed ID: 25489771
    [Abstract] [Full Text] [Related]

  • 20. Lower lip pits in a patient with van der Woude syndrome.
    Baghestani S, Sadeghi N, Yavarian M, Alghasi H.
    J Craniofac Surg; 2010 Sep 10; 21(5):1380-1. PubMed ID: 20818247
    [Abstract] [Full Text] [Related]

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