References
- Chiquet BT, Henry R, Burt A, Mulliken JB, Stal S, Blanton SH, Hecht JT. Nonsyndromic cleft lip and palate: CRISPLD genes and the folate gene pathway connection. Birth Defects Res A Clin Mol Teratol 2011;91:44–49. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21254358. doi:10.1002/bdra.20737.
- Leslie EJ, Marazita ML. Genetics of cleft lip and cleft palate. Am J Med Genet C Semin Med Genet. 2013;163C:246–258. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24124047 doi:10.1002/ajmg.c.31381.
- Rahimov F, Jugessur A, Murray JC. Genetics of nonsyndromic orofacial clefts. Cleft Palate-Craniofacial J. 2012;49:73–91. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21545302
- Cvjetkovic N, Maili L, Weymouth KS, Hashmi SS, Mulliken JB, Topczewski J, Letra A, Yuan Q, Blanton SH, Swindell EC, et al. Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family. Mol Genet Genomic Med. 2015;3:440–451. Available from: http://www.ncbi.nlm.nih.gov/pubmed/26436110 doi:10.1002/mgg3.155.
- Leslie EJ, Koboldt DC, Kang CJ, Ma L, Hecht JT, Wehby GL, Christensen K, Czeizel AE, Deleyiannis FW-B, Fulton RS, et al. IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families. Clin Genet. 2016;90:28–34. Available from: http://www.ncbi.nlm.nih.gov/pubmed/26346622 doi:10.1111/cge.12675.
- Gurramkonda VB, Syed AH, Murthy J, Lakkakula B. 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. Braz J Otorhinolaryngol. 2017;84:473–477. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28712851
- Stuppia L, Capogreco M, Marzo G, La Rovere D, Antonucci I, Gatta V, Palka G, Mortellaro C, Tetè S. Genetics of Syndromic and Nonsyndromic Cleft Lip and Palate. J Craniofac Surg. 2011;22:1722–1726. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21959420 doi:10.1097/SCS.0b013e31822e5e4d.
- Hlouskova A, Bielik P, Bonczek O, Balcar VJ, Šerý O. Mutations in AXIN2 gene as a risk factor for tooth agenesis and cancer: A review. Neuro Endocrinol Lett. 2017;38:131–137. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28759178
- Lammi L, Arte S, Somer M, Järvinen H, Lahermo P, Thesleff I, Pirinen S, Nieminen P. Mutations in AXIN2 Cause Familial Tooth Agenesis and Predispose to Colorectal Cancer. Am J Hum Genet. 2004;74:1043–1050. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15042511 doi:10.1086/386293.
- Liu H, Ding T, Zhan Y, Feng H. A Novel AXIN2 missense mutation is associated with non-syndromic oligodontia. Eisenberg L, editor. PLoS One [Internet]. 2015;10:e0138221. Available from: https://dx.plos.org/10.1371/journal.pone.0138221
- Kanzaki H, Ouchida M, Hanafusa H, Yano M, Suzuki H, Aoe M, et al. Single nucleotide polymorphism of the AXIN2 gene is preferentially associated with human lung cancer risk in a Japanese population. Int J Mol Med. 2006;18:279–284. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16820935 doi:10.3892/ijmm.18.2.279.
- Menezes R, Marazita ML, McHenry TG, Cooper ME, Bardi K, Brandon C, Letra A, Martin RA, Vieira AR. AXIS inhibition protein 2, orofacial clefts and a family history of cancer. J Am Dent Assoc. 2009;140:80–84. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19119171 doi:10.14219/jada.archive.2009.0022.
- Bastakoty D, Young PP. Wnt/β-catenin pathway in tissue injury: roles in pathology and therapeutic opportunities for regeneration. FASEB J. 2016;30:3271–3284. Available from: http://www.ncbi.nlm.nih.gov/pubmed/27335371 doi:10.1096/fj.201600502R.
- Aulehla A, Wehrle C, Brand-Saberi B, Kemler R, Gossler A, Kanzler B, Herrmann BG. Wnt3a plays a major role in the segmentation clock controlling somitogenesis. Dev Cell. 2003;4:395–406. Available from: https://www.sciencedirect.com/science/article/pii/S1534580703000558 doi:10.1016/S1534-5807(03)00055-8.
- Rafighdoost H, Hashemi M, Danesh H, Bizhani F, Bahari G, Taheri M. Association of single nucleotide polymorphisms in AXIN2, BMP4, and IRF6 with non-syndromic cleft lip with or without Cleft Palate in a sample of the southeast Iranian population. J Appl Oral Sci. 2017;25:650–656. Available from: http://www.ncbi.nlm.nih.gov/pubmed/29211286 doi:10.1590/1678-7757-2017-0191.
- Mostowska A, Hozyasz KK, Wójcicki P, Lasota A, Dunin-Wilczyńska I, Jagodziński PP. Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a polish population. Birth Defects Res Part A Clin Mol Teratol. 2012;94:943–950. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22887353 doi:10.1002/bdra.23056.
- Letra A, Menezes R, Granjeiro JM, Vieira AR. AXIN2 and CDH1 polymorphisms, tooth agenesis, and oral clefts. Birth Defect Res A. 2009;85:169–173. Available from: http://doi.wiley.com/10.1002/bdra.20489 doi:10.1002/bdra.20489.
- Bezerra JF, Oliveira GHM, Soares CD, Cardoso ML, Ururahy MAG, Neto FPF, Lima-Neto LG, Luchessi AD, Silbiger VN, Fajardo CM, et al. Genetic and non-genetic factors that increase the risk of non-syndromic cleft lip and/or palate development. Oral Dis. 2015;21:393–399. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25219684 doi:10.1111/odi.12292.
- Yuan Q, Blanton SH, Hecht JT. Genetic causes of nonsyndromic cleft lip with or without cleft palate. Adv Otorhinolaryngol. 2011;70:107–113. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21358192
- Vishnuvardhan V, Hegde M, R DM, Dharma RM. DNA sequencing for AXIN 2 (SNP 7591 and 7224837) gene polymorphisms in non-syndromic cleft lip and/or cleft palate in the local population. Int J Sci Res ISSN. 2015;6. Available from: www.ijsr.net
- Han Y, Zhou L, Ma L, Li D, Xu M, Yuan H, Ma J, Zhang W, Jiang H, Wu Y, et al. The axis inhibition protein 2 polymorphisms and non-syndromic orofacial clefts susceptibility in a Chinese Han population. J Oral Pathol Med. 2014;43:554–560. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24484320 doi:10.1111/jop.12162.
- Machado RA, de Freitas EM, de Aquino SN, Martelli DRB, Swerts MSO, Reis S. R D A, Persuhn DC, Moreira HSB, Dias VO, Coletta RD, et al. Clinical relevance of breast and gastric cancer-associated polymorphisms as potential susceptibility markers for oral clefts in the Brazilian population. BMC Med Genet. 2017;18:39. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28376813 doi:10.1186/s12881-017-0390-y.