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

Year Number of Results
1989 1
1991 3
1993 4
1994 5
1995 1
1996 6
1997 2
1998 7
1999 5
2001 4
2002 2
2003 2
2004 3
2005 3
2006 8
2007 7
2008 14
2009 5
2010 7
2011 14
2012 17
2013 13
2014 26
2015 26
2016 21
2017 15
2018 14
2019 16
2020 16
2021 5
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Article type
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Search Results

242 results
Results by year
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Page 1
Spina bifida.
Copp AJ, Adzick NS, Chitty LS, Fletcher JM, Holmbeck GN, Shaw GM. Copp AJ, et al. Among authors: chitty ls. Nat Rev Dis Primers. 2015 Apr 30;1:15007. doi: 10.1038/nrdp.2015.7. Nat Rev Dis Primers. 2015. PMID: 27189655 Free PMC article. Review.
Next-generation sequencing and the impact on prenatal diagnosis.
Mellis R, Chandler N, Chitty LS. Mellis R, et al. Among authors: chitty ls. Expert Rev Mol Diagn. 2018 Aug;18(8):689-699. doi: 10.1080/14737159.2018.1493924. Epub 2018 Jul 18. Expert Rev Mol Diagn. 2018. PMID: 29962246 Review.
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord J, McMullan DJ, Eberhardt RY, Rinck G, Hamilton SJ, Quinlan-Jones E, Prigmore E, Keelagher R, Best SK, Carey GK, Mellis R, Robart S, Berry IR, Chandler KE, Cilliers D, Cresswell L, Edwards SL, Gardiner C, Henderson A, Holden ST, Homfray T, Lester T, Lewis RA, Newbury-Ecob R, Prescott K, Quarrell OW, Ramsden SC, Roberts E, Tapon D, Tooley MJ, Vasudevan PC, Weber AP, Wellesley DG, Westwood P, White H, Parker M, Williams D, Jenkins L, Scott RH, Kilby MD, Chitty LS, Hurles ME, Maher ER; Prenatal Assessment of Genomes and Exomes Consortium. Lord J, et al. Among authors: chitty ls. Lancet. 2019 Feb 23;393(10173):747-757. doi: 10.1016/S0140-6736(18)31940-8. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712880 Free PMC article.
Cell-Free Fetal DNA Testing for Prenatal Diagnosis.
Drury S, Hill M, Chitty LS. Drury S, et al. Among authors: chitty ls. Adv Clin Chem. 2016;76:1-35. doi: 10.1016/bs.acc.2016.05.004. Epub 2016 Jun 28. Adv Clin Chem. 2016. PMID: 27645814 Review.
Non-invasive prenatal diagnosis and screening for monogenic disorders.
Scotchman E, Shaw J, Paternoster B, Chandler N, Chitty LS. Scotchman E, et al. Among authors: chitty ls. Eur J Obstet Gynecol Reprod Biol. 2020 Oct;253:320-327. doi: 10.1016/j.ejogrb.2020.08.001. Epub 2020 Aug 7. Eur J Obstet Gynecol Reprod Biol. 2020. PMID: 32907778 Review.
COngenital heart disease and the Diagnostic yield with Exome sequencing (CODE) study: prospective cohort study and systematic review.
Mone F, Eberhardt RY, Morris RK, Hurles ME, McMullan DJ, Maher ER, Lord J, Chitty LS, Giordano JL, Wapner RJ, Kilby MD; CODE Study Collaborators. Mone F, et al. Among authors: chitty ls. Ultrasound Obstet Gynecol. 2021 Jan;57(1):43-51. doi: 10.1002/uog.22072. Epub 2020 Dec 3. Ultrasound Obstet Gynecol. 2021. PMID: 32388881 Review.
242 results
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