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

Year Number of Results
1994 1
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2001 1
2003 1
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2010 1
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2012 3
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Page 1
ZIC2 in Holoprosencephaly.
Barratt KS, Arkell RM. Barratt KS, et al. Among authors: arkell rm. Adv Exp Med Biol. 2018;1046:269-299. doi: 10.1007/978-981-10-7311-3_14. Adv Exp Med Biol. 2018. PMID: 29442327 Review.
Overview of Rodent Zic Genes.
Diamand KEM, Barratt KS, Arkell RM. Diamand KEM, et al. Among authors: arkell rm. Adv Exp Med Biol. 2018;1046:179-207. doi: 10.1007/978-981-10-7311-3_10. Adv Exp Med Biol. 2018. PMID: 29442323 Review.
Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic Data.
Easteal S, Arkell RM, Balboa RF, Bellingham SA, Brown AD, Calma T, Cook MC, Davis M, Dawkins HJS, Dinger ME, Dobbie MS, Farlow A, Gwynne KG, Hermes A, Hoy WE, Jenkins MR, Jiang SH, Kaplan W, Leslie S, Llamas B, Mann GJ, McMorran BJ, McWhirter RE, Meldrum CJ, Nagaraj SH, Newman SJ, Nunn JS, Ormond-Parker L, Orr NJ, Paliwal D, Patel HR, Pearson G, Pratt GR, Rambaldini B, Russell LW, Savarirayan R, Silcocks M, Skinner JC, Souilmi Y, Vinuesa CG; National Centre for Indigenous Genomics; Baynam G. Easteal S, et al. Among authors: arkell rm. Am J Hum Genet. 2020 Aug 6;107(2):175-182. doi: 10.1016/j.ajhg.2020.06.005. Am J Hum Genet. 2020. PMID: 32763188 Free PMC article.
Zic2 mutation causes holoprosencephaly via disruption of NODAL signalling.
Houtmeyers R, Tchouate Gainkam O, Glanville-Jones HA, Van den Bosch B, Chappell A, Barratt KS, Souopgui J, Tejpar S, Arkell RM. Houtmeyers R, et al. Among authors: arkell rm. Hum Mol Genet. 2016 Sep 15;25(18):3946-3959. doi: 10.1093/hmg/ddw235. Epub 2016 Jul 27. Hum Mol Genet. 2016. PMID: 27466203
40 results