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NKX2.5 mutations in patients with non-syndromic congenital heart disease.
Gioli-Pereira L, Pereira AC, Mesquita SM, Xavier-Neto J, Lopes AA, Krieger JE. Gioli-Pereira L, et al. Among authors: pereira ac. Int J Cardiol. 2010 Feb 4;138(3):261-5. doi: 10.1016/j.ijcard.2008.08.035. Epub 2008 Dec 14. Int J Cardiol. 2010. PMID: 19073351
HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing?
Santos PC, Pereira AC, Cançado RD, Schettert IT, Sobreira TJ, Oliveira PS, Hirata RD, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM. Santos PC, et al. Among authors: pereira ac. Blood Cells Mol Dis. 2010 Dec 15;45(4):302-7. doi: 10.1016/j.bcmd.2010.08.008. Epub 2010 Sep 16. Blood Cells Mol Dis. 2010. PMID: 20843714
1,143 results