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

Year Number of Results
1969 1
1981 1
1982 2
1983 1
1992 2
1993 1
1994 4
1996 2
2004 1
2008 1
2009 1
2010 4
2011 2
2012 4
2013 2
2015 1
2019 2
2020 2
2021 0
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33 results
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Page 1
Direct imaging of short-range order and its impact on deformation in Ti-6Al.
Zhang R, Zhao S, Ophus C, Deng Y, Vachhani SJ, Ozdol B, Traylor R, Bustillo KC, Morris JW Jr, Chrzan DC, Asta M, Minor AM. Zhang R, et al. Among authors: traylor r. Sci Adv. 2019 Dec 13;5(12):eaax2799. doi: 10.1126/sciadv.aax2799. eCollection 2019 Dec. Sci Adv. 2019. PMID: 31853495 Free PMC article.
Clinical utility of chromosomal microarray analysis.
Ellison JW, Ravnan JB, Rosenfeld JA, Morton SA, Neill NJ, Williams MS, Lewis J, Torchia BS, Walker C, Traylor RN, Moles K, Miller E, Lantz J, Valentin C, Minier SL, Leiser K, Powell BR, Wilks TM, Shaffer LG. Ellison JW, et al. Among authors: traylor rn. Pediatrics. 2012 Nov;130(5):e1085-95. doi: 10.1542/peds.2012-0568. Epub 2012 Oct 15. Pediatrics. 2012. PMID: 23071206
Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 Microdeletions.
Traylor RN, Dobyns WB, Rosenfeld JA, Wheeler P, Spence JE, Bandholz AM, Bawle EV, Carmany EP, Powell CM, Hudson B, Schultz RA, Shaffer LG, Ballif BC. Traylor RN, et al. Mol Syndromol. 2012 Sep;3(3):102-112. doi: 10.1159/000342008. Epub 2012 Aug 23. Mol Syndromol. 2012. PMID: 23112752 Free PMC article.
MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways.
Paciorkowski AR, Traylor RN, Rosenfeld JA, Hoover JM, Harris CJ, Winter S, Lacassie Y, Bialer M, Lamb AN, Schultz RA, Berry-Kravis E, Porter BE, Falk M, Venkat A, Vanzo RJ, Cohen JS, Fatemi A, Dobyns WB, Shaffer LG, Ballif BC, Marsh ED. Paciorkowski AR, et al. Among authors: traylor rn. Neurogenetics. 2013 May;14(2):99-111. doi: 10.1007/s10048-013-0356-y. Epub 2013 Feb 7. Neurogenetics. 2013. PMID: 23389741 Free PMC article.
The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes.
Shaffer LG, Coppinger J, Morton SA, Alliman S, Burleson J, Traylor R, Walker C, Byerly S, Lamb AN, Schultz R, Ravnan JB, Kashork CD, Torchia BS, Sulpizio S, Sundin K, Schermer M, Adler K, Dallaire S, Ballif BC. Shaffer LG, et al. Among authors: traylor r. Prenat Diagn. 2011 Aug;31(8):778-87. doi: 10.1002/pd.2766. Epub 2011 Jun 21. Prenat Diagn. 2011. PMID: 21692086
33 results
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