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Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease.
Tomita-Mitchell A, Mahnke DK, Larson JM, Ghanta S, Feng Y, Simpson PM, Broeckel U, Duffy K, Tweddell JS, Grossman WJ, Routes JM, Mitchell ME. Tomita-Mitchell A, et al. Among authors: simpson pm. Physiol Genomics. 2010 Sep;42A(1):52-60. doi: 10.1152/physiolgenomics.00073.2010. Epub 2010 Jun 15. Physiol Genomics. 2010. PMID: 20551144 Free PMC article.
Human gene copy number spectra analysis in congenital heart malformations.
Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME. Tomita-Mitchell A, et al. Among authors: simpson pm. Physiol Genomics. 2012 May 1;44(9):518-41. doi: 10.1152/physiolgenomics.00013.2012. Epub 2012 Feb 7. Physiol Genomics. 2012. PMID: 22318994 Free PMC article.
Fontan fenestration closure and event-free survival.
Imielski BR, Woods RK, Mussatto KA, Cao Y, Simpson PM, Tweddell JS. Imielski BR, et al. Among authors: simpson pm. J Thorac Cardiovasc Surg. 2013 Jan;145(1):183-7. doi: 10.1016/j.jtcvs.2012.09.006. Epub 2012 Oct 9. J Thorac Cardiovasc Surg. 2013. PMID: 23062415 Free PMC article.
374 results