[1. Renju R, Varma BR, Kumar SJ, Kumaran P. Mandibulofacial dysostosis (Treacher Collins syndrome): A case report and review of literature. Contemp Clin Dent. 2014;5:532-53410.4103/0976-237X.142826422976725395774]Search in Google Scholar
[2. Kasat V, Baldawa R. Treacher Collins syndrome - A case report and review of literature. J Clin Exp Dent. 2011;3:e395-39910.4317/jced.3.e395]Search in Google Scholar
[3. Mohan RPS, Verma S, Agarwal N, Singh U. Treacher Collins syndrome: A case report. BMJ Case Rep. 2013;2013:bcr201300934110.1136/bcr-2013-009341366990223709540]Search in Google Scholar
[4. Panta P, Yaga US, Mengji AK, Radhika B, Rao MS. Treacher Collins syndrome - Case report and review. Oral Health Dent Manag. 2017;6:955-957.]Search in Google Scholar
[5. Katsanis SH, Jabs EW. Treacher Collins Syndrome, in: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle, 2004 [updated 2018], 1993-2019]Search in Google Scholar
[6. Weiner AM, Scampoli NL, Calcaterra NB. Fishing the molecular bases of Treacher Collins syndrome. PLoS One. 2012;7:e2957410.1371/journal.pone.0029574326625522295061]Search in Google Scholar
[7. Dixon J, Trainor P, Dixon MJ. Treacher Collins syndrome. OrthodCraniofac Res. 2007;10:88-9510.1111/j.1601-6343.2007.00388.x17552945]Search in Google Scholar
[8. Kumar T, Puri G, Konidena A, Arora N. Treacher Collins syndrome: A case report and review of literature. J Indian Acad Oral Med Radiol. 2015;27:488-49110.4103/0972-1363.170476]Search in Google Scholar
[9. Conte C, D’Apice MR, Rinaldi F, Gambardella S, Sangiuolo F, Novelli G. Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome. BMC Med Genet. 2011;12:12510.1186/1471-2350-12-125319923421951868]Search in Google Scholar
[10. Crauciuc GA, Tripon F, Bogliş A, Făgărăşan A, Bănescu C. Multiplex ligation dependent probe amplification - A useful, fast and cost-effective method for identification of small supernumerary marker chromosome in children with developmental delay and congenital heart defect. Rev Romana Med Lab. 2018;26:461-47010.2478/rrlm-2018-0032]Search in Google Scholar
[11. Bogliş A, Tripon F, Bănescu C. The utility of molecular genetic techniques in craniosynostosis cases associated with intellectual disability. Rev Romana Med Lab. 2018;26:471-47710.2478/rrlm-2018-0033]Search in Google Scholar
[12. Bănescu C. Do we really need genetic tests in current clinical practice? Rev Romana Med Lab. 2019;27:9-14]Search in Google Scholar
[13. Teber OA, Gillessen-Kaesbach G, Fischer S, et al. Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation. Eur J Hum Genet. 2004;12:879-89010.1038/sj.ejhg.520126015340364]Search in Google Scholar
[14. Schlump JU, Stein A, Hehr U, et al. Treacher Collins syndrome: clinical implications for the paediatrician-a new mutation in a severely affected newborn and comparison with three further patients with the same mutation, and review of the literature. Eur J Pediatr. 2012; 171:1611-161810.1007/s00431-012-1776-722729243]Search in Google Scholar
[15. Horiuchi K, Ariga T, Fujioka H, et al. Mutational analysis of the TCOF1 gene in 11 Japanese patients with Treacher Collins Syndrome and mechanism of mutagenesis. Am J Med Genet A. 2005; 134:363-36710.1002/ajmg.a.3035715759264]Search in Google Scholar
[16. Beygo J, K. Buiting, S. Seland, et al. First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome. Mol Syndromol. 2012;2:53–5910.1159/000335545332666222712005]Search in Google Scholar
[17. Yan Z, Lu Y, Wang Y, et al. Identification of a novel TCOF1 mutation in a Chinese family with Treacher Collins syndrome. Exp Ther Med. 2018;16:2645–265010.3892/etm.2018.6446612248930186496]Search in Google Scholar
[18. Caluseriu O, Lowry BR, McLeod R, et al. The Hutterite variant of Treacher Collins syndrome: a 28-year-old story solved. Am. J. Med. Genet. 2013;161A:2855-285910.1002/ajmg.a.3617224108658]Search in Google Scholar
[19. Vincent M, Genevieve D, Ostertag A, et al. Treacher Collins syndrome: a clinical and molecular study based on a large series of patients. Genet. Med. 2016;18:49-56]Search in Google Scholar
[20. Vincent M, Collet C, Verloes A, et al. Large deletions encompassing the TCOF1and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability. Eur J Hum Genet. 2014;22:52-5610.1038/ejhg.2013.98386542023695276]Search in Google Scholar
[21. Ulusal S, Gürkan H, Vatansever U, Kürkçü K, Tozkir H, Acunaş B. A case of treachercollins syndrome. Balkan J Med Genet. 2013;16:77–8010.2478/bjmg-2013-0036400142024778568]Search in Google Scholar