MOLECULAR GENETICS OF CLEFT LIP AND PALATE: A REVIEW.
作者信息
Oboli G O, Chukwuma D I, Fagbule O F, Abe E O, Adisa A O
机构信息
College of Medicine, University of Ibadan, Ibadan.
Department of Periodontology and Community Dentistry, University College Hospital, Ibadan.
出版信息
Ann Ib Postgrad Med. 2020 Jun;18(1):S16-S21.
Abstract
摘要
相似文献
1
MOLECULAR GENETICS OF CLEFT LIP AND PALATE: A REVIEW.
Ann Ib Postgrad Med. 2020 Jun;18(1):S16-S21.
2
An update on the aetiology of orofacial clefts.
Hong Kong Med J. 2004 Oct;10(5):331-6.
3
[Association of the genetic variation of (MSX1-7) and non syndromic cleft lip palate in Chilean subjects].
Rev Med Chil. 1998 Jun;126(6):637-45.
4
[Environmental factors of non-syndromic cleft lip and palate].
Hua Xi Kou Qiang Yi Xue Za Zhi. 2019 Oct 1;37(5):547-550. doi: 10.7518/hxkq.2019.05.018.
5
Dermatoglyphics and Cheiloscopy as Key Tools in Resolving the Genetic Correlation of Inheritance Patterns in Cleft Lip and Palate Patients: An Assessment of 160 Patients.
Cleft Palate Craniofac J. 2017 Sep;54(5):588-594. doi: 10.1597/15-168. Epub 2016 May 25.
6
Genetics of cleft lip and/or cleft palate: association with other common anomalies.
Eur J Med Genet. 2014 Aug;57(8):381-93. doi: 10.1016/j.ejmg.2014.04.003. Epub 2014 Apr 21.
7
Unraveling human cleft lip and palate research.
J Dent Res. 2008 Feb;87(2):119-25. doi: 10.1177/154405910808700202.
8
Genetics of cleft lip and palate revisited.
J Clin Pediatr Dent. 2003 Summer;27(4):311-20. doi: 10.17796/jcpd.27.4.k7j3628944237392.
9
Incidence of cleft lip, cleft palate, and cleft lip and palate among races: a review.
Cleft Palate J. 1987 Jul;24(3):216-25.
10
Treatment outcome in cleft lip and palate: issues and perspectives.
Crit Rev Oral Biol Med. 1999;10(2):225-39. doi: 10.1177/10454411990100020801.
引用本文的文献
1
Meta-analysis and systematic review for the genetic basis of cleft lip and palate.
J Oral Biol Craniofac Res. 2025 Jan-Feb;15(1):146-152. doi: 10.1016/j.jobcr.2024.12.012. Epub 2025 Jan 8.
2
Proteomic analysis illustrates the potential involvement of motor proteins in cleft palate development.
Sci Rep. 2024 Sep 19;14(1):21868. doi: 10.1038/s41598-024-73036-0.
3
Peripheral giant cell granuloma in a child with ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome: a case report.
BMC Oral Health. 2024 Aug 13;24(1):936. doi: 10.1186/s12903-024-04585-z.
本文引用的文献
1
p63 establishes epithelial enhancers at critical craniofacial development genes.
Sci Adv. 2019 May 1;5(5):eaaw0946. doi: 10.1126/sciadv.aaw0946. eCollection 2019 May.
2
Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1.
Bone. 2018 Sep;114:125-136. doi: 10.1016/j.bone.2018.06.013. Epub 2018 Jun 19.
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.
J Med Genet. 2018 Jul;55(7):449-458. doi: 10.1136/jmedgenet-2017-105110. Epub 2018 Mar 2.
4
Blepharocheilodontic syndrome is a CDH1 pathway-related disorder due to mutations in CDH1 and CTNND1.
Genet Med. 2017 Sep;19(9):1013-1021. doi: 10.1038/gim.2017.11. Epub 2017 Mar 16.
5
The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery.
Nat Genet. 2016 Jun;48(6):648-56. doi: 10.1038/ng.3558. Epub 2016 May 9.
6
Epidemiology, Etiology, and Treatment of Isolated Cleft Palate.
Front Physiol. 2016 Mar 1;7:67. doi: 10.3389/fphys.2016.00067. eCollection 2016.
7
IRF6 is the mediator of TGFβ3 during regulation of the epithelial mesenchymal transition and palatal fusion.
Sci Rep. 2015 Aug 4;5:12791. doi: 10.1038/srep12791.
8
Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome.
J Med Genet. 2015 Feb;52(2):104-10. doi: 10.1136/jmedgenet-2014-102677. Epub 2014 Nov 20.
9
Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability.
Am J Med Genet A. 2014 Jul;164A(7):1622-6. doi: 10.1002/ajmg.a.36498. Epub 2014 Mar 26.
10
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.
Am J Hum Genet. 2014 Feb 6;94(2):295-302. doi: 10.1016/j.ajhg.2014.01.001. Epub 2014 Jan 23.
Zotero 插件