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

Year Number of Results
1962 1
1963 1
1964 8
1965 7
1966 2
1967 1
1968 1
1969 1
1970 4
1971 1
1972 2
1974 1
1975 2
1976 2
1977 3
1978 4
1979 1
1981 1
1982 3
1983 3
1984 1
1985 1
1986 2
1987 4
1988 2
1990 3
1992 2
1993 1
1994 2
1996 1
1999 1
2000 1
2001 2
2003 3
2005 2
2006 1
2007 1
2008 3
2009 2
2011 2
2012 3
2013 54
2014 83
2015 87
2016 94
2017 54
2018 58
2019 75
2020 84
2021 70
2022 57
2023 64
2024 46
2025 5

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778 results

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Page 1
[Trisomy 18 syndrome: A case report].
Saldarriaga W, Rengifo-Miranda H, Ramírez-Cheyne J. Saldarriaga W, et al. Rev Chil Pediatr. 2016 Mar-Apr;87(2):129-36. doi: 10.1016/j.rchipe.2015.08.006. Epub 2015 Oct 12. Rev Chil Pediatr. 2016. PMID: 26460083 Free article. Spanish.
INTRODUCTION: The trisomy 18 syndrome occurs due to the presence of an extra chromosome 18 in most cases. ...X-ray findings showed formation of missing teeth, with late eruption being concluded. CONCLUSIONS: In cases of trisomy 18 syndrome
INTRODUCTION: The trisomy 18 syndrome occurs due to the presence of an extra chromosome 18 in most cases. ...X-ray find …
Surveillance guidelines for children with trisomy 18.
Kepple JW, Fishler KP, Peeples ES. Kepple JW, et al. Am J Med Genet A. 2021 Apr;185(4):1294-1303. doi: 10.1002/ajmg.a.62097. Epub 2021 Feb 2. Am J Med Genet A. 2021. PMID: 33527722 Review.
A tumor profile in Edwards syndrome (trisomy 18).
Satgé D, Nishi M, Sirvent N, Vekemans M. Satgé D, et al. Am J Med Genet C Semin Med Genet. 2016 Sep;172(3):296-306. doi: 10.1002/ajmg.c.31511. Epub 2016 Jul 30. Am J Med Genet C Semin Med Genet. 2016. PMID: 27474103 Review.
Trisomy 13 and 18-Prevalence and mortality-A multi-registry population based analysis.
Goel N, Morris JK, Tucker D, de Walle HEK, Bakker MK, Kancherla V, Marengo L, Canfield MA, Kallen K, Lelong N, Camelo JL, Stallings EB, Jones AM, Nance A, Huynh MP, Martínez-Fernández ML, Sipek A, Pierini A, Nembhard WN, Goetz D, Rissmann A, Groisman B, Luna-Muñoz L, Szabova E, Lapchenko S, Zarante I, Hurtado-Villa P, Martinez LE, Tagliabue G, Landau D, Gatt M, Dastgiri S, Morgan M. Goel N, et al. Am J Med Genet A. 2019 Dec;179(12):2382-2392. doi: 10.1002/ajmg.a.61365. Epub 2019 Sep 30. Am J Med Genet A. 2019. PMID: 31566869 Free PMC article.
Holoprosencephaly.
Society for Maternal-Fetal Medicine (SMFM); Monteagudo A. Society for Maternal-Fetal Medicine (SMFM), et al. Am J Obstet Gynecol. 2020 Dec;223(6):B13-B16. doi: 10.1016/j.ajog.2020.08.178. Epub 2020 Nov 7. Am J Obstet Gynecol. 2020. PMID: 33168217 Review. No abstract available.
Anatomy of trisomy 18.
Roberts W, Zurada A, Zurada-ZieliŃSka A, Gielecki J, Loukas M. Roberts W, et al. Clin Anat. 2016 Jul;29(5):628-32. doi: 10.1002/ca.22725. Epub 2016 May 3. Clin Anat. 2016. PMID: 27087248 Review.
Non-invasive prenatal testing.
Harraway J. Harraway J. Aust Fam Physician. 2017 Oct;46(10):735-739. Aust Fam Physician. 2017. PMID: 29036772 Free article.
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
van der Meij KRM, Sistermans EA, Macville MVE, Stevens SJC, Bax CJ, Bekker MN, Bilardo CM, Boon EMJ, Boter M, Diderich KEM, de Die-Smulders CEM, Duin LK, Faas BHW, Feenstra I, Haak MC, Hoffer MJV, den Hollander NS, Hollink IHIM, Jehee FS, Knapen MFCM, Kooper AJA, van Langen IM, Lichtenbelt KD, Linskens IH, van Maarle MC, Oepkes D, Pieters MJ, Schuring-Blom GH, Sikkel E, Sikkema-Raddatz B, Smeets DFCM, Srebniak MI, Suijkerbuijk RF, Tan-Sindhunata GM, van der Ven AJEM, van Zelderen-Bhola SL, Henneman L, Galjaard RH, Van Opstal D, Weiss MM; Dutch NIPT Consortium. van der Meij KRM, et al. Am J Hum Genet. 2019 Dec 5;105(6):1091-1101. doi: 10.1016/j.ajhg.2019.10.005. Epub 2019 Nov 7. Am J Hum Genet. 2019. PMID: 31708118 Free PMC article.
778 results