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Journal Abstract Search

400 related items for PubMed ID: 21959420

  • 1. Genetics of syndromic and nonsyndromic cleft lip and palate.
    Stuppia L, Capogreco M, Marzo G, La Rovere D, Antonucci I, Gatta V, Palka G, Mortellaro C, Tetè S.
    J Craniofac Surg; 2011 Sep; 22(5):1722-6. PubMed ID: 21959420
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  • 2. Orofacial clefting: update on the role of genetics.
    Ghassibe M, Bayet B, Revencu N, Desmyter L, Verellen-Dumoulin C, Gillerot Y, Deggouj N, Vanwijck R, Vikkula M, CL/P Study Group.
    B-ENT; 2006 Sep; 2 Suppl 4():20-4. PubMed ID: 17366841
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  • 4. [Van-der-Woude Syndrome].
    Del Frari B, Amort M, Janecke AR, Schutte BC, Piza-Katzer H.
    Klin Padiatr; 2008 Sep; 220(1):26-8. PubMed ID: 18095255
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  • 5. Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes.
    Pegelow M, Peyrard-Janvid M, Zucchelli M, Fransson I, Larson O, Kere J, Larsson C, Karsten A.
    Eur J Orthod; 2008 Apr; 30(2):169-75. PubMed ID: 18209213
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  • 6. 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
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  • 8. Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing.
    Khandelwal KD, Ishorst N, Zhou H, Ludwig KU, Venselaar H, Gilissen C, Thonissen M, van Rooij IA, Dreesen K, Steehouwer M, van de Vorst M, Bloemen M, van Beusekom E, Roosenboom J, Borstlap W, Admiraal R, Dormaar T, Schoenaers J, Vander Poorten V, Hens G, Verdonck A, Bergé S, Roeleveldt N, Vriend G, Devriendt K, Brunner HG, Mangold E, Hoischen A, van Bokhoven H, Carels CE.
    J Dent Res; 2017 Feb; 96(2):179-185. PubMed ID: 27834299
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  • 9. Novel lip pit phenotypes and mutations of IRF6 in Van der Woude syndrome patients from Pakistan.
    Malik S, Wilcox ER, Naz S.
    Clin Genet; 2014 May; 85(5):487-91. PubMed ID: 23713753
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  • 10. Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort.
    Wang Y, Sun Y, Huang Y, Pan Y, Jia Z, Ma L, Ma L, Lan F, Zhou Y, Shi J, Yang X, Zhang L, Jiang H, Jiang M, Yin A, Cheng J, Wang L, Yang Y, Shi B.
    Gene; 2016 Aug 15; 588(1):69-73. PubMed ID: 27129939
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  • 12. Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.
    Nikopensius T, Jagomägi T, Krjutskov K, Tammekivi V, Saag M, Prane I, Piekuse L, Akota I, Barkane B, Krumina A, Ambrozaityte L, Matuleviciene A, Kucinskiene ZA, Lace B, Kucinskas V, Metspalu A.
    Birth Defects Res A Clin Mol Teratol; 2010 Sep 15; 88(9):748-56. PubMed ID: 20672350
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  • 13. Significant association between IRF6 820G->A and non-syndromic cleft lip with or without cleft palate in the Thai population.
    Srichomthong C, Siriwan P, Shotelersuk V.
    J Med Genet; 2005 Jul 15; 42(7):e46. PubMed ID: 15994871
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  • 14. A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude syndrome.
    Miñones-Suárez L, Mas-Vidal A, Fernandez-Toral J, Llano-Rivas I, González-García M.
    Pediatr Dermatol; 2012 Jul 15; 29(6):768-70. PubMed ID: 21995291
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  • 15. The genetic factors contributing to the risk of cleft lip-cleft palate and their clinical utility.
    Askarian S, Gholami M, Khalili-Tanha G, Tehrani NC, Joudi M, Khazaei M, Ferns GA, Hassanian SM, Avan A, Joodi M.
    Oral Maxillofac Surg; 2023 Jun 15; 27(2):177-186. PubMed ID: 35426585
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  • 20. 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 15; 52(5):e161-7. PubMed ID: 25489771
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