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Journal Abstract Search

338 related items for PubMed ID: 36493769

  • 1.
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  • 2. Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans.
    Lansdon LA, Darbro BW, Petrin AL, Hulstrand AM, Standley JM, Brouillette RB, Long A, Mansilla MA, Cornell RA, Murray JC, Houston DW, Manak JR.
    Genetics; 2018 Jan; 208(1):283-296. PubMed ID: 29162626
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  • 3. 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; 55(7):449-458. PubMed ID: 29500247
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  • 4. A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk.
    Younkin SG, Scharpf RB, Schwender H, Parker MM, Scott AF, Marazita ML, Beaty TH, Ruczinski I.
    BMC Genet; 2014 Feb 14; 15():24. PubMed ID: 24528994
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  • 6. A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.
    Leslie EJ, Carlson JC, Shaffer JR, Feingold E, Wehby G, Laurie CA, Jain D, Laurie CC, Doheny KF, McHenry T, Resick J, Sanchez C, Jacobs J, Emanuele B, Vieira AR, Neiswanger K, Lidral AC, Valencia-Ramirez LC, Lopez-Palacio AM, Valencia DR, Arcos-Burgos M, Czeizel AE, Field LL, Padilla CD, Cutiongco-de la Paz EM, Deleyiannis F, Christensen K, Munger RG, Lie RT, Wilcox A, Romitti PA, Castilla EE, Mereb JC, Poletta FA, Orioli IM, Carvalho FM, Hecht JT, Blanton SH, Buxó CJ, Butali A, Mossey PA, Adeyemo WL, James O, Braimah RO, Aregbesola BS, Eshete MA, Abate F, Koruyucu M, Seymen F, Ma L, de Salamanca JE, Weinberg SM, Moreno L, Murray JC, Marazita ML.
    Hum Mol Genet; 2016 Jul 01; 25(13):2862-2872. PubMed ID: 27033726
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  • 8. Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.
    Jezewski PA, Vieira AR, Nishimura C, Ludwig B, Johnson M, O'Brien SE, Daack-Hirsch S, Schultz RE, Weber A, Nepomucena B, Romitti PA, Christensen K, Orioli IM, Castilla EE, Machida J, Natsume N, Murray JC.
    J Med Genet; 2003 Jun 01; 40(6):399-407. PubMed ID: 12807959
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  • 9. Genetics of cleft lip and cleft palate.
    Leslie EJ, Marazita ML.
    Am J Med Genet C Semin Med Genet; 2013 Nov 01; 163C(4):246-58. PubMed ID: 24124047
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  • 10. 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 Nov 01; 2 Suppl 4():20-4. PubMed ID: 17366841
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  • 11. Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts.
    Stanier P, Moore GE.
    Hum Mol Genet; 2004 Apr 01; 13 Spec No 1():R73-81. PubMed ID: 14722155
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  • 12. Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts.
    Conte F, Oti M, Dixon J, Carels CE, Rubini M, Zhou H.
    Hum Genet; 2016 Jan 01; 135(1):41-59. PubMed ID: 26561393
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  • 13. Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate.
    Leslie EJ, Murray JC.
    Clin Genet; 2013 Nov 01; 84(5):496-500. PubMed ID: 22978696
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  • 14. Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.
    Ludwig KU, Böhmer AC, Bowes J, Nikolic M, Ishorst N, Wyatt N, Hammond NL, Gölz L, Thieme F, Barth S, Schuenke H, Klamt J, Spielmann M, Aldhorae K, Rojas-Martinez A, Nöthen MM, Rada-Iglesias A, Dixon MJ, Knapp M, Mangold E.
    Hum Mol Genet; 2017 Feb 15; 26(4):829-842. PubMed ID: 28087736
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  • 15. Two novel genes TOX3 and COL21A1 in large extended Malay families with nonsyndromic cleft lip and/or palate.
    Mohamad Shah NS, Sulong S, Wan Sulaiman WA, Halim AS.
    Mol Genet Genomic Med; 2019 May 15; 7(5):e635. PubMed ID: 30924295
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  • 16. Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation.
    Simioni M, Araujo TK, Monlleo IL, Maurer-Morelli CV, Gil-da-Silva-Lopes VL.
    J Hum Genet; 2015 Jan 15; 60(1):17-25. PubMed ID: 25391604
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