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

Year Number of Results
1991 1
1993 1
1996 3
1997 1
1998 1
2000 2
2002 1
2003 1
2004 2
2005 1
2006 1
2007 5
2008 2
2009 5
2010 4
2011 2
2012 5
2013 4
2014 2
2015 1
2016 2
2017 3
2018 1
2019 1
2020 2
2021 1
2022 2
2024 0

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53 results

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Page 1
Human Germline Genome Editing.
Ormond KE, Mortlock DP, Scholes DT, Bombard Y, Brody LC, Faucett WA, Garrison NA, Hercher L, Isasi R, Middleton A, Musunuru K, Shriner D, Virani A, Young CE. Ormond KE, et al. Among authors: mortlock dp. Am J Hum Genet. 2017 Aug 3;101(2):167-176. doi: 10.1016/j.ajhg.2017.06.012. Am J Hum Genet. 2017. PMID: 28777929 Free PMC article. Review.
Limb development: molecular dysmorphology is at hand!
Innis JW, Mortlock DP. Innis JW, et al. Among authors: mortlock dp. Clin Genet. 1998 May;53(5):337-48. doi: 10.1111/j.1399-0004.1998.tb02744.x. Clin Genet. 1998. PMID: 9660051 Free article. Review.
Control of BMP gene expression by long-range regulatory elements.
Pregizer S, Mortlock DP. Pregizer S, et al. Among authors: mortlock dp. Cytokine Growth Factor Rev. 2009 Oct-Dec;20(5-6):509-15. doi: 10.1016/j.cytogfr.2009.10.011. Epub 2009 Nov 8. Cytokine Growth Factor Rev. 2009. PMID: 19900834 Free PMC article. Review.
CRISPR/Cas9 engineering of albino cystinuria Type A mice.
Beckermann TM, Welch RC, Williams FM, Mortlock DP, Sha F, Ikizler TA, Woodard LE, Wilson MH. Beckermann TM, et al. Among authors: mortlock dp. Genesis. 2020 May;58(5):e23357. doi: 10.1002/dvg.23357. Epub 2020 Feb 20. Genesis. 2020. PMID: 32078250 Free PMC article.
Calcific aortic valve disease: a consensus summary from the Alliance of Investigators on Calcific Aortic Valve Disease.
Yutzey KE, Demer LL, Body SC, Huggins GS, Towler DA, Giachelli CM, Hofmann-Bowman MA, Mortlock DP, Rogers MB, Sadeghi MM, Aikawa E. Yutzey KE, et al. Among authors: mortlock dp. Arterioscler Thromb Vasc Biol. 2014 Nov;34(11):2387-93. doi: 10.1161/ATVBAHA.114.302523. Epub 2014 Sep 4. Arterioscler Thromb Vasc Biol. 2014. PMID: 25189570 Free PMC article. Review.
Recurrent tissue-specific mtDNA mutations are common in humans.
Samuels DC, Li C, Li B, Song Z, Torstenson E, Boyd Clay H, Rokas A, Thornton-Wells TA, Moore JH, Hughes TM, Hoffman RD, Haines JL, Murdock DG, Mortlock DP, Williams SM. Samuels DC, et al. Among authors: mortlock dp. PLoS Genet. 2013 Nov;9(11):e1003929. doi: 10.1371/journal.pgen.1003929. Epub 2013 Nov 7. PLoS Genet. 2013. PMID: 24244193 Free PMC article.
53 results