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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1947 2
1948 2
1949 8
1950 4
1951 6
1952 4
1953 8
1954 10
1955 10
1956 4
1957 4
1958 8
1959 11
1960 15
1961 16
1962 14
1963 12
1964 25
1965 23
1966 23
1967 37
1968 33
1969 33
1970 42
1971 36
1972 33
1973 30
1974 49
1975 43
1976 31
1977 38
1978 35
1979 35
1980 29
1981 34
1982 38
1983 33
1984 28
1985 29
1986 29
1987 39
1988 23
1989 37
1990 37
1991 35
1992 36
1993 43
1994 36
1995 48
1996 49
1997 32
1998 41
1999 25
2000 31
2001 41
2002 48
2003 35
2004 43
2005 41
2006 56
2007 54
2008 60
2009 53
2010 56
2011 69
2012 85
2013 91
2014 110
2015 91
2016 92
2017 81
2018 98
2019 85
2020 94
2021 110
2022 102
2023 118
2024 116
2025 94
2026 33

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3,119 results

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Page 1
Treacher Collins Syndrome: Genetics, Clinical Features and Management.
Marszałek-Kruk BA, Wójcicki P, Dowgierd K, Śmigiel R. Marszałek-Kruk BA, et al. Genes (Basel). 2021 Sep 9;12(9):1392. doi: 10.3390/genes12091392. Genes (Basel). 2021. PMID: 34573374 Free PMC article. Review.
Treacher Collins syndrome (TCS) is associated with abnormal differentiation of the first and second pharyngeal arches, occurring during fetal development. ...TCS occurs in the general population at a frequency of 1 in 50,000 live births. Four subtypes of T …
Treacher Collins syndrome (TCS) is associated with abnormal differentiation of the first and second pharyngeal arches, …
Treacher Collins Syndrome.
Aljerian A, Gilardino MS. Aljerian A, et al. Clin Plast Surg. 2019 Apr;46(2):197-205. doi: 10.1016/j.cps.2018.11.005. Epub 2019 Jan 30. Clin Plast Surg. 2019. PMID: 30851751 Review.
Treacher Collins syndrome is a rare genetic disorder of craniofacial development with a highly variable phenotype. ...
Treacher Collins syndrome is a rare genetic disorder of craniofacial development with a highly variable phenotype. ...
Treacher Collins syndrome.
Dixon MJ. Dixon MJ. Hum Mol Genet. 1996;5 Spec No:1391-6. doi: 10.1093/hmg/5.supplement_1.1391. Hum Mol Genet. 1996. PMID: 8875242 Review.
Treacher Collins syndrome is an autosomal dominant disorder of craniofacial development, the features of which include conductive hearing loss and cleft palate. ...
Treacher Collins syndrome is an autosomal dominant disorder of craniofacial development, the features of which include …
Treacher Collins syndrome.
Dixon J, Trainor P, Dixon MJ. Dixon J, et al. Orthod Craniofac Res. 2007 May;10(2):88-95. doi: 10.1111/j.1601-6343.2007.00388.x. Orthod Craniofac Res. 2007. PMID: 17552945 Review.
Treacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development which results from loss-of-function mutations in the gene TCOF1. ...
Treacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development which results from loss-o …
Treacher Collins syndrome.
Dixon MJ. Dixon MJ. J Med Genet. 1995 Oct;32(10):806-8. doi: 10.1136/jmg.32.10.806. J Med Genet. 1995. PMID: 8558560 Free PMC article. Review. No abstract available.
Treacher Collins syndrome.
Marsh KL, Dixon MJ. Marsh KL, et al. Adv Otorhinolaryngol. 2000;56:53-9. doi: 10.1159/000059083. Adv Otorhinolaryngol. 2000. PMID: 10868214 Review. No abstract available.
Prevention methods for Treacher Collins syndrome: A systematic review.
Guo P, Pan B, Jiang H, Yang Q, He L, Lin L. Guo P, et al. Int J Pediatr Otorhinolaryngol. 2020 Jul;134:110062. doi: 10.1016/j.ijporl.2020.110062. Epub 2020 Apr 21. Int J Pediatr Otorhinolaryngol. 2020. PMID: 32361149
OBJECTIVES: Treacher Collins syndrome (TCS) is a severe congenital mandibulofacial dysostosis that occurs one in every 50,000 births. ...METHODS: A systematic review was conducted through an electronic search of PubMed, EMBASE and Web of Science …
OBJECTIVES: Treacher Collins syndrome (TCS) is a severe congenital mandibulofacial dysostosis that occurs …
Treacher Collins syndrome (mandibulofacial dysostosis).
Fuente del Campo A, Martinez Elizondo M, Arnaud E. Fuente del Campo A, et al. Clin Plast Surg. 1994 Oct;21(4):613-23. Clin Plast Surg. 1994. PMID: 7813160 Review.
Treacher Collins syndrome is a complex congenital malformation. The most important manifestations of this syndrome are hypoplastic or absent malar bone, centrofacial over-projection, eyelid coloboma, and micrognathia. ...
Treacher Collins syndrome is a complex congenital malformation. The most important manifestations of this syndrome …
Treacher Collins Syndrome: A Systematic Review of Evidence-Based Treatment and Recommendations.
Plomp RG, van Lieshout MJS, Joosten KFM, Wolvius EB, van der Schroeff MP, Versnel SL, Poublon RML, Mathijssen IMJ. Plomp RG, et al. Plast Reconstr Surg. 2016 Jan;137(1):191-204. doi: 10.1097/PRS.0000000000001896. Plast Reconstr Surg. 2016. PMID: 26710023
BACKGROUND: No reviews or guidelines are available on evidence-based treatment for the multidisciplinary approach in Treacher Collins syndrome. The authors' aim is to provide an evidence-based review of multidisciplinary treatment of Treacher Collin …
BACKGROUND: No reviews or guidelines are available on evidence-based treatment for the multidisciplinary approach in Treacher Coll …
Treacher Collins syndrome: New insights from animal models.
Tse WK. Tse WK. Int J Biochem Cell Biol. 2016 Dec;81(Pt A):44-47. doi: 10.1016/j.biocel.2016.10.016. Epub 2016 Oct 21. Int J Biochem Cell Biol. 2016. PMID: 27777025 Review.
Treacher Collins syndrome (TCS, OMIM: 154500), an autosomal-dominant craniofacial developmental syndrome that occurs in 1 out of every 50,000 live births, is characterized by craniofacial malformation. ...
Treacher Collins syndrome (TCS, OMIM: 154500), an autosomal-dominant craniofacial developmental syndrome that oc …
3,119 results