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

Year Number of Results
1964 1
1965 2
1969 1
1970 1
1971 1
1973 1
1975 1
1976 3
1977 2
1978 2
1979 3
1980 1
1981 3
1982 2
1983 4
1984 5
1985 8
1987 6
1988 7
1989 8
1990 11
1991 9
1992 11
1993 7
1994 14
1995 14
1996 10
1997 15
1998 21
1999 17
2000 15
2001 18
2002 17
2003 16
2004 12
2005 20
2006 19
2007 30
2008 24
2009 19
2010 24
2011 31
2012 51
2013 53
2014 66
2015 59
2016 70
2017 63
2018 53
2019 70
2020 65
2021 53
2022 58
2023 55
2024 22

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1,026 results

Results by year

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Page 1
Trisomy 13.
Pereira EM. Pereira EM. Pediatr Rev. 2023 Jan 1;44(1):53-54. doi: 10.1542/pir.2022-005517. Pediatr Rev. 2023. PMID: 36587017 No abstract available.
Interdisciplinary care of children with trisomy 13 and 18.
Weaver MS, Anderson V, Beck J, Delaney JW, Ellis C, Fletcher S, Hammel J, Haney S, Macfadyen A, Norton B, Rickard M, Robinson JA, Sewell R, Starr L, Birge ND. Weaver MS, et al. Am J Med Genet A. 2021 Mar;185(3):966-977. doi: 10.1002/ajmg.a.62051. Epub 2020 Dec 31. Am J Med Genet A. 2021. PMID: 33381915 Review.
Children with trisomy 13 and 18 (previously deemed "incompatible with life") are living longer, warranting a comprehensive overview of their unique comorbidities and complex care needs. ...
Children with trisomy 13 and 18 (previously deemed "incompatible with life") are living longer, warranting a comprehensive ove …
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.
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.
The aim of the study is to determine the prevalence, outcomes, and survival (among live births [LB]), in pregnancies diagnosed with trisomy 13 (T13) and 18 (T18), by congenital anomaly register and region. ...
The aim of the study is to determine the prevalence, outcomes, and survival (among live births [LB]), in pregnancies diagnosed with triso …
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.
The number of trisomies 21 (239, 0.33%), 18 (49, 0.07%), and 13 (55, 0.08%) found in this study is comparable to earlier studies, but the Positive Predictive Values (PPV)-96% for trisomy 21, 98% for trisomy 18, and 53% for trisomy 13-were higher than expected. Findi …
The number of trisomies 21 (239, 0.33%), 18 (49, 0.07%), and 13 (55, 0.08%) found in this study is comparable to earlier studies, but the Po …
Analysis of cell-free DNA in maternal blood in screening for aneuploidies: updated meta-analysis.
Gil MM, Accurti V, Santacruz B, Plana MN, Nicolaides KH. Gil MM, et al. Ultrasound Obstet Gynecol. 2017 Sep;50(3):302-314. doi: 10.1002/uog.17484. Epub 2017 Jul 27. Ultrasound Obstet Gynecol. 2017. PMID: 28397325 Free article. Updated. Review.
In a total of 563 cases of trisomy 18 and 222 013 non-trisomy 18 singleton pregnancies, the weighted pooled DR and FPR were 97.9% (95% CI, 94.9-99.1%) and 0.04% (95% CI, 0.03-0.07%), respectively. In a total of 119 cases of trisomy 13 and 212 883 non-trisomy …
In a total of 563 cases of trisomy 18 and 222 013 non-trisomy 18 singleton pregnancies, the weighted pooled DR and FPR were 97.9% (95% CI, 9 …
Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies.
Rose NC, Barrie ES, Malinowski J, Jenkins GP, McClain MR, LaGrave D, Leung ML; ACMG Professional Practice and Guidelines Committee. Electronic address: documents@acmg.net. Rose NC, et al. Genet Med. 2022 Jul;24(7):1379-1391. doi: 10.1016/j.gim.2022.03.019. Epub 2022 May 24. Genet Med. 2022. PMID: 35608568 Free article. Review.
METHODS: Medline (PubMed) and Embase were used to identify studies examining detection of Down syndrome (T21), trisomy 18 (T18), trisomy 13 (T13), sex chromosome aneuploidies, rare autosomal trisomies, copy number variants, and maternal conditions, as well as studie …
METHODS: Medline (PubMed) and Embase were used to identify studies examining detection of Down syndrome (T21), trisomy 18 (T18), trisomy …
Trisomies.
Levy PA, Marion R. Levy PA, et al. Pediatr Rev. 2018 Feb;39(2):104-106. doi: 10.1542/pir.2016-0198. Pediatr Rev. 2018. PMID: 29437136 No abstract available.
Polydactyly.
Society for Maternal-Fetal Medicine; Rac MWF, McKinney J, Gandhi M. Society for Maternal-Fetal Medicine, et al. Am J Obstet Gynecol. 2019 Dec;221(6):B13-B15. doi: 10.1016/j.ajog.2019.09.023. Am J Obstet Gynecol. 2019. PMID: 31787158 No abstract available.
Trisomy 13 mosaicism.
Cammarata-Scalisi F, Araque D, Ramírez R, Guaran L, Silva GD. Cammarata-Scalisi F, et al. Bol Med Hosp Infant Mex. 2019;76(5):246-250. doi: 10.24875/BMHIM.19000003. Bol Med Hosp Infant Mex. 2019. PMID: 31536039 English.
BACKGROUND: Trisomy 13 is a chromosomal alteration with an incidence of 1 in 10,000 to 20,000 births. ...CASE REPORTS: The clinical and cytogenetic findings of two new cases of trisomy 13 mosaicism are described. CONCLUSIONS: The importance of prenatal …
BACKGROUND: Trisomy 13 is a chromosomal alteration with an incidence of 1 in 10,000 to 20,000 births. ...CASE REPORTS: The cli …
1,026 results