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Journal Abstract Search

429 related items for PubMed ID: 29489415

  • 21. Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.
    Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, Natsume N, Yoshiura K, Vieira AR, Orioli IM, Castilla EE, Moreno L, Arcos-Burgos M, Lidral AC, Field LL, Liu YE, Ray A, Goldstein TH, Schultz RE, Shi M, Johnson MK, Kondo S, Schutte BC, Marazita ML, Murray JC.
    N Engl J Med; 2004 Aug 19; 351(8):769-80. PubMed ID: 15317890
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  • 22. Ethnic Differences in the Brazilian Population Influence the Impact of BMP4 Genetic Variants on Susceptibility of Nonsyndromic Orofacial Clefts.
    Rocha de Oliveira LQ, de Souza Nicolau HC, Barbosa Martelli DR, Martelli-Júnior H, Scariot R, Ayroza Rangel ALC, de Almeida Reis SR, Coletta RD, Machado RA.
    Cleft Palate Craniofac J; 2024 Oct 19; 61(10):1701-1712. PubMed ID: 37272066
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  • 23. Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P).
    Houdayer C, Bonaïti-Pellié C, Erguy C, Soupre V, Dondon MG, Bürglen L, Cougoureux E, Couderc R, Vazquez MP, Bahuau M.
    Am J Med Genet; 2001 Nov 15; 104(1):86-92. PubMed ID: 11746036
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  • 24. Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.
    Leslie EJ, Mansilla MA, Biggs LC, Schuette K, Bullard S, Cooper M, Dunnwald M, Lidral AC, Marazita ML, Beaty TH, Murray JC.
    Birth Defects Res A Clin Mol Teratol; 2012 Nov 15; 94(11):934-42. PubMed ID: 23008150
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  • 25. Medical sequencing of candidate genes for nonsyndromic cleft lip and palate.
    Vieira AR, Avila JR, Daack-Hirsch S, Dragan E, Félix TM, Rahimov F, Harrington J, Schultz RR, Watanabe Y, Johnson M, Fang J, O'Brien SE, Orioli IM, Castilla EE, Fitzpatrick DR, Jiang R, Marazita ML, Murray JC.
    PLoS Genet; 2005 Dec 15; 1(6):e64. PubMed ID: 16327884
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  • 26. 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 15; 96(2):179-185. PubMed ID: 27834299
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  • 29. Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population.
    Ludwig KU, Wahle P, Reutter H, Paredes-Zenteno M, Muñoz-Jimenez SG, Ortiz-Lopez R, Böhmer AC, Tessmann P, Nowak S, Nöthen MM, Knapp M, Rojas-Martinez A, Mangold E.
    Birth Defects Res A Clin Mol Teratol; 2014 Jan 15; 100(1):43-7. PubMed ID: 24382704
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  • 34. Polymorphisms at 1q32, 8q24, and 17q22 loci are associated with nonsyndromic cleft lip with or without cleft palate risk in the Slovak population.
    Salagovic J, Klimcakova L, Zabavnikova M, Behunova J, Hudakova T, Fedeles J, Molnarova A, Podracka L.
    Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2017 Jun 15; 161(2):152-157. PubMed ID: 28422192
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  • 36. Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.
    Mangold E, Böhmer AC, Ishorst N, Hoebel AK, Gültepe P, Schuenke H, Klamt J, Hofmann A, Gölz L, Raff R, Tessmann P, Nowak S, Reutter H, Hemprich A, Kreusch T, Kramer FJ, Braumann B, Reich R, Schmidt G, Jäger A, Reiter R, Brosch S, Stavusis J, Ishida M, Seselgyte R, Moore GE, Nöthen MM, Borck G, Aldhorae KA, Lace B, Stanier P, Knapp M, Ludwig KU.
    Am J Hum Genet; 2016 Apr 07; 98(4):755-62. PubMed ID: 27018475
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  • 37. SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients.
    de Assis NA, Nowak S, Ludwig KU, Reutter H, Vollmer J, Heilmann S, Kluck N, Lauster C, Braumann B, Reich RH, Hemprich A, Knapp M, Wienker TF, Kramer FJ, Hoffmann P, Nöthen MM, Mangold E.
    Int J Pediatr Otorhinolaryngol; 2011 Jan 07; 75(1):49-52. PubMed ID: 21044801
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  • 38. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes.
    Basha M, Demeer B, Revencu N, Helaers R, Theys S, Bou Saba S, Boute O, Devauchelle B, Francois G, Bayet B, Vikkula M.
    J Med Genet; 2018 Jul 07; 55(7):449-458. PubMed ID: 29500247
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  • 39. [Association between polymorphism of IRF6 rs2235371 locus and nonsyndromic cleft lip with or without cleft palate].
    Li MJ, Zhu WL, Wang Y, Guo JZ, Li SQ, Li Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr 07; 29(2):149-54. PubMed ID: 22487822
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