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

Year Number of Results
2014 1
2015 2
2016 6
2017 3
2018 2
2019 1
2020 3
2021 1
2023 1
2024 1

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15 results

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Page 1
Carrier screening for single gene disorders.
Rose NC, Wick M. Rose NC, et al. Semin Fetal Neonatal Med. 2018 Apr;23(2):78-84. doi: 10.1016/j.siny.2017.06.001. Epub 2017 Jun 29. Semin Fetal Neonatal Med. 2018. PMID: 28669541 Review.
Family Sense-Making After a Down Syndrome Diagnosis.
Clark L, Canary HE, McDougle K, Perkins R, Tadesse R, Holton AE. Clark L, et al. Qual Health Res. 2020 Oct;30(12):1783-1797. doi: 10.1177/1049732320935836. Epub 2020 Jul 3. Qual Health Res. 2020. PMID: 32618226 Free PMC article.
Whole Genome Sequencing and Newborn Screening.
Botkin JR, Rothwell E. Botkin JR, et al. Curr Genet Med Rep. 2016 Mar 1;4(1):1-6. doi: 10.1007/s40142-016-0084-3. Epub 2016 Feb 1. Curr Genet Med Rep. 2016. PMID: 27134803 Free PMC article.
Deliberative Discussion Focus Groups.
Rothwell E, Anderson R, Botkin JR. Rothwell E, et al. Qual Health Res. 2016 May;26(6):734-40. doi: 10.1177/1049732315591150. Epub 2015 Jun 15. Qual Health Res. 2016. PMID: 26078330 Free PMC article.
Parental permission for pilot newborn screening research: guidelines from the NBSTRN.
Botkin JR, Lewis MH, Watson MS, Swoboda KJ, Anderson R, Berry SA, Bonhomme N, Brosco JP, Comeau AM, Goldenberg A, Goldman E, Therrell B, Levy-Fisch J, Tarini B, Wilfond B; Bioethics and Legal Work Group of the Newborn Screening Translational Research Network. Botkin JR, et al. Pediatrics. 2014 Feb;133(2):e410-7. doi: 10.1542/peds.2013-2271. Epub 2014 Jan 6. Pediatrics. 2014. PMID: 24394680 Free PMC article.
15 results