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Journal Abstract Search
131 related items for PubMed ID: 38796699
21. 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; 61(10):1701-1712. PubMed ID: 37272066 [Abstract] [Full Text] [Related]
22. Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios. Bishop MR, Diaz Perez KK, Sun M, Ho S, Chopra P, Mukhopadhyay N, Hetmanski JB, Taub MA, Moreno-Uribe LM, Valencia-Ramirez LC, Restrepo Muñeton CP, Wehby G, Hecht JT, Deleyiannis F, Weinberg SM, Wu-Chou YH, Chen PK, Brand H, Epstein MP, Ruczinski I, Murray JC, Beaty TH, Feingold E, Lipinski RJ, Cutler DJ, Marazita ML, Leslie EJ. Am J Hum Genet; 2020 Jul 02; 107(1):124-136. PubMed ID: 32574564 [Abstract] [Full Text] [Related]
23. Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting. Diaz Perez KK, Curtis SW, Sanchis-Juan A, Zhao X, Head T, Ho S, Carter B, McHenry T, Bishop MR, Valencia-Ramirez LC, Restrepo C, Hecht JT, Uribe LM, Wehby G, Weinberg SM, Beaty TH, Murray JC, Feingold E, Marazita ML, Cutler DJ, Epstein MP, Brand H, Leslie EJ. Genet Med; 2023 Oct 02; 25(10):100918. PubMed ID: 37330696 [Abstract] [Full Text] [Related]
24. Orofacial clefts embryology, classification, epidemiology, and genetics. Nasreddine G, El Hajj J, Ghassibe-Sabbagh M. Mutat Res Rev Mutat Res; 2021 Oct 02; 787():108373. PubMed ID: 34083042 [Abstract] [Full Text] [Related]
25. Secondary Genome-Wide Association Study Using Novel Analytical Strategies Disentangle Genetic Components of Cleft Lip and/or Cleft Palate in 1q32.2. Yang Y, Suzuki A, Iwata J, Jun G. Genes (Basel); 2020 Oct 29; 11(11):. PubMed ID: 33137956 [Abstract] [Full Text] [Related]
26. Gene×environment associations in orofacial clefting. Marazita ML. Curr Top Dev Biol; 2023 Oct 29; 152():169-192. PubMed ID: 36707211 [Abstract] [Full Text] [Related]
27. Whole-genome sequencing in a pair of monozygotic twins with discordant cleft lip and palate subtypes. Takahashi M, Hosomichi K, Yamaguchi T, Nagahama R, Yoshida H, Maki K, Marazita ML, Weinberg SM, Tajima A. Oral Dis; 2018 Oct 29; 24(7):1303-1309. PubMed ID: 29873870 [Abstract] [Full Text] [Related]
28. The evolution of human genetic studies of cleft lip and cleft palate. Marazita ML. Annu Rev Genomics Hum Genet; 2012 Oct 29; 13():263-83. PubMed ID: 22703175 [Abstract] [Full Text] [Related]
29. 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 29; 135(1):41-59. PubMed ID: 26561393 [Abstract] [Full Text] [Related]
30. Genetic variants of 20q12 contributed to non-syndromic orofacial clefts susceptibility. Yin X, Ma L, Li Y, Xu M, Wang W, Wang H, Yuan H, Du Y, Li S, Ma J, Jiang H, Wang L, Zhang W, Pan Y. Oral Dis; 2017 Jan 29; 23(1):50-54. PubMed ID: 27537108 [Abstract] [Full Text] [Related]
31. Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a Polish population. Mostowska A, Hozyasz KK, Wójcicki P, Lasota A, Dunin-Wilczyńska I, Jagodziński PP. Birth Defects Res A Clin Mol Teratol; 2012 Nov 29; 94(11):943-50. PubMed ID: 22887353 [Abstract] [Full Text] [Related]
32. Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population. He M, Bian Z. PLoS One; 2016 Nov 29; 11(7):e0159940. PubMed ID: 27459192 [Abstract] [Full Text] [Related]
33. Studies with Wnt genes and nonsyndromic cleft lip and palate. Menezes R, Letra A, Kim AH, Küchler EC, Day A, Tannure PN, Gomes da Motta L, Paiva KB, Granjeiro JM, Vieira AR. Birth Defects Res A Clin Mol Teratol; 2010 Nov 29; 88(11):995-1000. PubMed ID: 20890934 [Abstract] [Full Text] [Related]
34. Cellular and developmental basis of orofacial clefts. Ji Y, Garland MA, Sun B, Zhang S, Reynolds K, McMahon M, Rajakumar R, Islam MS, Liu Y, Chen Y, Zhou CJ. Birth Defects Res; 2020 Nov 29; 112(19):1558-1587. PubMed ID: 32725806 [Abstract] [Full Text] [Related]
35. Genetic models and approaches to study orofacial clefts. Leslie EJ. Oral Dis; 2022 Jul 29; 28(5):1327-1338. PubMed ID: 34923716 [Abstract] [Full Text] [Related]
36. RERE deficiency contributes to the development of orofacial clefts in humans and mice. Kim BJ, Zaveri HP, Kundert PN, Jordan VK, Scott TM, Carmichael J, Scott DA. Hum Mol Genet; 2021 May 12; 30(7):595-602. PubMed ID: 33772547 [Abstract] [Full Text] [Related]
37. IRF6 rs2235375 single nucleotide polymorphism is associated with isolated non-syndromic cleft palate but not with cleft lip with or without palate in South Indian population. Gurramkonda VB, Syed AH, Murthy J, Lakkakula BVKS. Braz J Otorhinolaryngol; 2018 May 12; 84(4):473-477. PubMed ID: 28712851 [Abstract] [Full Text] [Related]
38. Functional Effects of SNPs in MYH9 and Risks of Nonsyndromic Orofacial Clefts. Wang Y, Li D, Xu Y, Ma L, Lu Y, Wang Z, Wang L, Zhang W, Pan Y. J Dent Res; 2018 Apr 12; 97(4):388-394. PubMed ID: 29207917 [Abstract] [Full Text] [Related]
39. Embryology and epidemiology of cleft lip and palate. Bernheim N, Georges M, Malevez C, De Mey A, Mansbach A. B-ENT; 2006 Apr 12; 2 Suppl 4():11-9. PubMed ID: 17366840 [Abstract] [Full Text] [Related]