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362 related items for PubMed ID: 12807959
21. Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region. Slayton RL, Williams L, Murray JC, Wheeler JJ, Lidral AC, Nishimura CJ. Cleft Palate Craniofac J; 2003 May; 40(3):274-9. PubMed ID: 12733956 [Abstract] [Full Text] [Related]
23. PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations. Avila JR, Jezewski PA, Vieira AR, Orioli IM, Castilla EE, Christensen K, Daack-Hirsch S, Romitti PA, Murray JC. Am J Med Genet A; 2006 Dec 01; 140(23):2562-70. PubMed ID: 17089422 [Abstract] [Full Text] [Related]
24. Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations. Ingersoll RG, Hetmanski J, Park JW, Fallin MD, McIntosh I, Wu-Chou YH, Chen PK, Yeow V, Chong SS, Cheah F, Sull JW, Jee SH, Wang H, Wu T, Murray T, Huang S, Ye X, Jabs EW, Redett R, Raymond G, Scott AF, Beaty TH. Eur J Hum Genet; 2010 Jun 01; 18(6):726-32. PubMed ID: 20087401 [Abstract] [Full Text] [Related]
25. 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 [Abstract] [Full Text] [Related]
26. Family-based analysis of MSX1 haplotypes for association with oral clefts. Fallin MD, Hetmanski JB, Park J, Scott AF, Ingersoll R, Fuernkranz HA, McIntosh I, Beaty TH. Genet Epidemiol; 2003 Sep 19; 25(2):168-75. PubMed ID: 12916025 [Abstract] [Full Text] [Related]
27. Testing candidate genes for non-syndromic oral clefts using a case-parent trio design. Beaty TH, Hetmanski JB, Zeiger JS, Fan YT, Liang KY, VanderKolk CA, McIntosh I. Genet Epidemiol; 2002 Jan 19; 22(1):1-11. PubMed ID: 11754469 [Abstract] [Full Text] [Related]
28. MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population. Tongkobpetch S, Siriwan P, Shotelersuk V. J Hum Genet; 2006 Jan 19; 51(8):671. PubMed ID: 16868654 [Abstract] [Full Text] [Related]
29. Cleft lip and/or palate with monogenic autosomal recessive transmission in Pyrenees shepherd dogs. Kemp C, Thiele H, Dankof A, Schmidt G, Lauster C, Fernahl G, Lauster R. Cleft Palate Craniofac J; 2009 Jan 19; 46(1):81-8. PubMed ID: 19115787 [Abstract] [Full Text] [Related]
30. Parent-of-origin effects for MSX1 in a Chilean population with nonsyndromic cleft lip/palate. Suazo J, Santos JL, Jara L, Blanco R. Am J Med Genet A; 2010 Aug 19; 152A(8):2011-6. PubMed ID: 20635363 [Abstract] [Full Text] [Related]
31. CHD7 gene and non-syndromic cleft lip and palate. Félix TM, Hanshaw BC, Mueller R, Bitoun P, Murray JC. Am J Med Genet A; 2006 Oct 01; 140(19):2110-4. PubMed ID: 16763960 [Abstract] [Full Text] [Related]
32. Rescue of cleft palate in Msx1-deficient mice by transgenic Bmp4 reveals a network of BMP and Shh signaling in the regulation of mammalian palatogenesis. Zhang Z, Song Y, Zhao X, Zhang X, Fermin C, Chen Y. Development; 2002 Sep 01; 129(17):4135-46. PubMed ID: 12163415 [Abstract] [Full Text] [Related]
34. Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families. Schultz RE, Cooper ME, Daack-Hirsch S, Shi M, Nepomucena B, Graf KA, O'Brien EK, O'Brien SE, Marazita ML, Murray JC. Am J Med Genet A; 2004 Feb 15; 125A(1):17-22. PubMed ID: 14755461 [Abstract] [Full Text] [Related]
35. Linkage and linkage disequilibrium searched for between non-syndromic cleft palate and four candidate loci. Koillinen H, Ollikainen V, Rautio J, Hukki J, Kere J. J Med Genet; 2003 Jun 15; 40(6):464-8. PubMed ID: 12807970 [No Abstract] [Full Text] [Related]
36. Novel human mutation and CRISPR/Cas genome-edited mice reveal the importance of C-terminal domain of MSX1 in tooth and palate development. Mitsui SN, Yasue A, Masuda K, Naruto T, Minegishi Y, Oyadomari S, Noji S, Imoto I, Tanaka E. Sci Rep; 2016 Dec 05; 6():38398. PubMed ID: 27917906 [Abstract] [Full Text] [Related]
37. A miRNA-binding-site SNP of MSX1 is Associated with NSOC Susceptibility. Ma L, Xu M, Li D, Han Y, Wang Z, Yuan H, Ma J, Zhang W, Jiang H, Pan Y, Wang L. J Dent Res; 2014 Jun 05; 93(6):559-64. PubMed ID: 24603642 [Abstract] [Full Text] [Related]
38. 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 Jun 05; 2 Suppl 4():20-4. PubMed ID: 17366841 [Abstract] [Full Text] [Related]
39. Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes. Lansdon LA, Dickinson A, Arlis S, Liu H, Hlas A, Hahn A, Bonde G, Long A, Standley J, Tyryshkina A, Wehby G, Lee NR, Daack-Hirsch S, Mohlke K, Girirajan S, Darbro BW, Cornell RA, Houston DW, Murray JC, Manak JR. Am J Hum Genet; 2023 Jan 05; 110(1):71-91. PubMed ID: 36493769 [Abstract] [Full Text] [Related]
40. Association of MSX1 with nonsyndromic cleft lip and palate in a Colombian population. Otero L, Gutiérrez S, Cháves M, Vargas C, Bérmudez L. Cleft Palate Craniofac J; 2007 Nov 05; 44(6):653-6. PubMed ID: 18177186 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]