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Journal Abstract Search

331 related items for PubMed ID: 10645953

  • 1. 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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  • 2. Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.
    Schutte BC, Sander A, Malik M, Murray JC.
    Genomics; 1996 Sep 15; 36(3):507-14. PubMed ID: 8884274
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  • 3. 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
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  • 4. 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 21; 9(10):747-52. PubMed ID: 11781685
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  • 5. 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 21; 57(2):72-6. PubMed ID: 10445358
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  • 7. 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 Apr 21; 19(3):128-34. PubMed ID: 10589394
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  • 9. Novel mutations in the IRF6 gene for Van der Woude syndrome.
    Wang X, Liu J, Zhang H, Xiao M, Li J, Yang C, Lin X, Wu Z, Hu L, Kong X.
    Hum Genet; 2003 Oct 21; 113(5):382-6. PubMed ID: 12920575
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  • 10. 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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  • 11. 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 10; 3(4):575-8. PubMed ID: 8069301
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  • 12. Altered regulation of cell migration in IRF6-mutated orofacial cleft patients-derived primary cells reveals a novel role of Rho GTPases in cleft/lip palate development.
    Ghassibe-Sabbagh M, El Hajj J, Al Saneh M, El Baba N, Abou Issa J, Al Haddad M, El Atat O, Sabbagh J, Abou Chebel N, El-Sibai M.
    Cells Dev; 2021 Jun 10; 166():203674. PubMed ID: 33994351
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  • 18. Van der Woude syndrome: a review of 11 cases seen at the Lagos University Teaching Hospital.
    James O, Adeyemo WL, Emeka CI, Ogunlewe MO, Ladeinde AL, Butali A.
    Afr J Paediatr Surg; 2014 Jun 10; 11(1):52-5. PubMed ID: 24647295
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