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Journal Abstract Search

121 related items for PubMed ID: 11961959

  • 1. [Association between cleft lip/palate phenotype and non syndrome microsatellite markers located in 6p, 17q and 19q].
    Carreño H, Suazo J, Paredes M, Solá J, Valenzuela J, Blanco R.
    Rev Med Chil; 2002 Jan; 130(1):35-44. PubMed ID: 11961959
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  • 2. [Association of non-syndromic cleft lip and cleft palate with microsatellite markers located in 6p].
    Carreño H, Paredes M, Téllez G, Palomino H, Blanco R.
    Rev Med Chil; 1999 Oct; 127(10):1189-98. PubMed ID: 10835735
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  • 3. Association between 10 microsatellite markers and nonsyndromic cleft lip palate in the Chilean population.
    Blanco R, Suazo J, Santos JL, Paredes M, Sung H, Carreño H, Jara L.
    Cleft Palate Craniofac J; 2004 Mar; 41(2):163-7. PubMed ID: 14989688
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  • 5. [Possible association due to linkage disequilibrium of TGFA, RARA and BCL3 with nonsyndromic cleft lip with or without cleft palate in the Chilean population].
    Suazo J, Santos JL, Silva V, Jara L, Palomino H, Blanco R.
    Rev Med Chil; 2005 Sep; 133(9):1051-8. PubMed ID: 16311697
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  • 6. [Evaluation of the association between microsatellite markers located on 6p22-25 and no syndromic cleft lip palate using the case-parents trio design in Chilean population ].
    Blanco R, Suazo J, Santos JL, Carreño H, Paredes M, Jara L, Eltit F.
    Rev Med Chil; 2003 Jul; 131(7):765-72. PubMed ID: 14513697
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  • 9. Lack of evidence for a significant association between nonsyndromic cleft lip with or without cleft palate and the retinoic acid receptor alpha gene in the Japanese population.
    Kanno K, Suzuki Y, Yang X, Yamada A, Aoki Y, Kure S, Matsubara Y.
    J Hum Genet; 2002 Jul; 47(6):269-74. PubMed ID: 12111375
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  • 11. No evidence for linkage and association between 4q microsatellite markers and nonsyndromic cleft lip and palate in chilean case-parents trios.
    Blanco R, Suazo J, Santos JL, Carreño H, Palomino H, Jara L.
    Cleft Palate Craniofac J; 2005 May; 42(3):267-71. PubMed ID: 15865460
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  • 13. ACSS2 gene variant associated with cleft lip and palate in two independent Hispanic populations.
    Dodhia S, Celis K, Aylward A, Cai Y, Fontana ME, Trespalacios A, Hoffman DC, Alfonso HO, Eisig SB, Su GH, Chung WK, Haddad J.
    Laryngoscope; 2017 Oct; 127(10):E336-E339. PubMed ID: 28543373
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  • 14. [Association study on microsatellite polymorphisms of MSX1 gene and nonsyndromic cleft lip and palate].
    Wu PA, Li YL, Fan GZ, Wang K.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):325-7. PubMed ID: 17557248
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  • 15. Study of the 12q13 region in nonsyndromic cleft lip with or without cleft palate.
    Martinelli M, Carinci F, Morselli PG, Palmieri A, Girardi A, Clauser L, Spinelli G, Scapoli L.
    Int J Immunopathol Pharmacol; 2011 Jun; 24(2 Suppl):21-4. PubMed ID: 21781441
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  • 16. Association of IFT88 gene variants with nonsyndromic cleft lip with or without cleft palate.
    Barba A, Urbina C, Maili L, Greives MR, Blackwell SJ, Mulliken JB, Chiquet B, Blanton SH, Hecht JT, Letra A.
    Birth Defects Res; 2019 Jul 01; 111(11):659-665. PubMed ID: 30953423
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  • 17. Nonsyndromic cleft lip and palate: four chromosomal regions of interest.
    Blanton SH, Bertin T, Patel S, Stal S, Mulliken JB, Hecht JT.
    Am J Med Genet A; 2004 Feb 15; 125A(1):28-37. PubMed ID: 14755463
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  • 18. The CRISPLD2 gene is involved in cleft lip and/or cleft palate in a Chinese population.
    Shen X, Liu RM, Yang L, Wu H, Li PQ, Liang YL, Xie XD, Yao T, Zhang TT, Yu M.
    Birth Defects Res A Clin Mol Teratol; 2011 Oct 15; 91(10):918-24. PubMed ID: 21800413
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  • 19. Association between NOGGIN and SPRY2 polymorphisms and nonsyndromic cleft lip with or without cleft palate.
    Song T, Shi J, Guo Q, Lv K, Jiao X, Hu T, Sun X, Fu S.
    Am J Med Genet A; 2015 Jan 15; 167A(1):137-41. PubMed ID: 25339627
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  • 20. Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.
    Ludwig KU, Ahmed ST, Böhmer AC, Sangani NB, Varghese S, Klamt J, Schuenke H, Gültepe P, Hofmann A, Rubini M, Aldhorae KA, Steegers-Theunissen RP, Rojas-Martinez A, Reiter R, Borck G, Knapp M, Nakatomi M, Graf D, Mangold E, Peters H.
    PLoS Genet; 2016 Mar 15; 12(3):e1005914. PubMed ID: 26968009
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