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Year Number of Results
1949 2
1950 1
1951 1
1952 1
1953 3
1954 2
1955 1
1956 1
1958 3
1960 1
1961 2
1962 2
1963 1
1964 3
1965 5
1966 2
1967 7
1968 1
1969 1
1970 2
1971 3
1974 4
1975 6
1976 3
1977 7
1978 5
1979 7
1980 4
1981 6
1982 2
1983 3
1984 5
1985 5
1986 5
1987 7
1988 6
1989 7
1990 9
1991 16
1992 5
1993 19
1994 10
1995 27
1996 16
1997 13
1998 13
1999 5
2000 9
2001 5
2002 18
2003 15
2004 20
2005 10
2006 18
2007 24
2008 23
2009 26
2010 12
2011 23
2012 38
2013 40
2014 38
2015 27
2016 30
2017 18
2018 27
2019 27
2020 32
2021 42
2022 24
2023 31
2024 17

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787 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.
Katsanis SH, Jabs EW. Katsanis SH, et al. 2004 Jul 20 [updated 2020 Aug 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2004 Jul 20 [updated 2020 Aug 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301704 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Treacher Collins syndrome (TCS) is characterized by bilateral and symmetric downslanting palpebral fissures, malar hypoplasia, micrognathia, and external ear abnormalities. ...The age of maxillomandibular reconstruction varies by sev …
CLINICAL CHARACTERISTICS: Treacher Collins syndrome (TCS) is characterized by bilateral and symmetric downslanting palp …
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 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.
THE TREACHER-COLLINS SYNDROME.
FERNANDEZ AO, RONIS ML. FERNANDEZ AO, et al. Arch Otolaryngol. 1964 Nov;80:505-20. doi: 10.1001/archotol.1964.00750040519006. Arch Otolaryngol. 1964. PMID: 14216013 Review. No abstract available.
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 Review.
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 occurs in
Treacher collins syndrome.
Chang CC, Steinbacher DM. Chang CC, et al. Semin Plast Surg. 2012 May;26(2):83-90. doi: 10.1055/s-0032-1320066. Semin Plast Surg. 2012. PMID: 23633935 Free PMC article.
Treacher Collins syndrome is a genetic disorder resulting in congenital craniofacial malformation. ...Here the authors review the features, genetics, and treatment of Treacher Collins syndrome....
Treacher Collins syndrome is a genetic disorder resulting in congenital craniofacial malformation. ...Here the authors
787 results