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

Year Number of Results
1966 1
1969 1
1972 1
1976 1
1978 1
1982 3
1987 1
1989 2
1992 2
1998 1
1999 2
2004 1
2005 1
2006 2
2007 1
2008 1
2009 2
2010 3
2011 1
2012 6
2013 3
2014 2
2015 1
2016 6
2017 22
2018 11
2019 2
2020 1
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Similar Articles for PMID: 29437136

76 results
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Page 1
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.
Prenatal reflex DNA screening for trisomy 21, 18 and 13.
Wald NJ. Wald NJ. Expert Rev Mol Diagn. 2018 May;18(5):399-401. doi: 10.1080/14737159.2018.1462703. Epub 2018 Apr 24. Expert Rev Mol Diagn. 2018. PMID: 29633889 Review. No abstract available.
ISUOG updated consensus statement on the impact of cfDNA aneuploidy testing on screening policies and prenatal ultrasound practice.
Salomon LJ, Alfirevic Z, Audibert F, Kagan KO, Paladini D, Yeo G, Raine-Fenning N; ISUOG Clinical Standards Committee. Salomon LJ, et al. Ultrasound Obstet Gynecol. 2017 Jun;49(6):815-816. doi: 10.1002/uog.17483. Ultrasound Obstet Gynecol. 2017. PMID: 28573775 Free article. No abstract available.
Massively Parallel Sequencing (MPS) of Cell-Free Fetal DNA (cffDNA) for Trisomies 21, 18, and 13 in Twin Pregnancies.
Du E, Feng C, Cao Y, Yao Y, Lu J, Zhang Y. Du E, et al. Twin Res Hum Genet. 2017 Jun;20(3):242-249. doi: 10.1017/thg.2017.23. Epub 2017 May 9. Twin Res Hum Genet. 2017. PMID: 28485265
Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
Petersen AK, Cheung SW, Smith JL, Bi W, Ward PA, Peacock S, Braxton A, Van Den Veyver IB, Breman AM. Petersen AK, et al. Am J Obstet Gynecol. 2017 Dec;217(6):691.e1-691.e6. doi: 10.1016/j.ajog.2017.10.005. Epub 2017 Oct 13. Am J Obstet Gynecol. 2017. PMID: 29032050 Free article.
The Combining Effects of Cell-Free Circulating Tumor DNA of Breast Tumor to the Noninvasive Prenatal Testing Results: A Simulating Investigation.
Cai YH, Yao GY, Chen LJ, Gan HY, Ye CS, Yang XX. Cai YH, et al. DNA Cell Biol. 2018 Jul;37(7):626-633. doi: 10.1089/dna.2017.4112. Epub 2018 Jun 29. DNA Cell Biol. 2018. PMID: 29957029
The contingent use of cell-free fetal DNA for prenatal screening of trisomies 21, 18, 13 in pregnant women within a national health service: A budget impact analysis.
Prefumo F, Paolini D, Speranza G, Palmisano M, Dionisi M, Camurri L. Prefumo F, et al. PLoS One. 2019 Jun 12;14(6):e0218166. doi: 10.1371/journal.pone.0218166. eCollection 2019. PLoS One. 2019. PMID: 31188879 Free PMC article.
Who Is the Next "Baby Doe?" From Trisomy 21 to Trisomy 13 and 18 and Beyond.
Kett JC. Kett JC. Pediatrics. 2020 Aug;146(Suppl 1):S9-S12. doi: 10.1542/peds.2020-0818D. Pediatrics. 2020. PMID: 32737226
Payer decision making for next-generation sequencing-based genetic tests: insights from cell-free DNA prenatal screening.
Dervan AP, Deverka PA, Trosman JR, Weldon CB, Douglas MP, Phillips KA. Dervan AP, et al. Genet Med. 2017 May;19(5):559-567. doi: 10.1038/gim.2016.145. Epub 2016 Sep 22. Genet Med. 2017. PMID: 27657682 Free PMC article.
Prenatal counseling and parental decision-making following a fetal diagnosis of trisomy 13 or 18.
Winn P, Acharya K, Peterson E, Leuthner S. Winn P, et al. J Perinatol. 2018 Jul;38(7):788-796. doi: 10.1038/s41372-018-0107-x. Epub 2018 May 8. J Perinatol. 2018. PMID: 29740195 Free article.
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