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Page 1
Molecular and cellular basis of congenital heart disease.
Sander TL, Klinkner DB, Tomita-Mitchell A, Mitchell ME. Sander TL, et al. Among authors: mitchell me. Pediatr Clin North Am. 2006 Oct;53(5):989-1009, x. doi: 10.1016/j.pcl.2006.08.010. Pediatr Clin North Am. 2006. PMID: 17027620 Review.
The molecular basis of congenital heart disease.
Mitchell ME, Sander TL, Klinkner DB, Tomita-Mitchell A. Mitchell ME, et al. Semin Thorac Cardiovasc Surg. 2007 Fall;19(3):228-37. doi: 10.1053/j.semtcvs.2007.07.013. Semin Thorac Cardiovasc Surg. 2007. PMID: 17983950 Review.
Investigation of somatic NKX2-5 mutations in congenital heart disease.
Draus JM Jr, Hauck MA, Goetsch M, Austin EH 3rd, Tomita-Mitchell A, Mitchell ME. Draus JM Jr, et al. Among authors: mitchell me. J Med Genet. 2009 Feb;46(2):115-22. doi: 10.1136/jmg.2008.060277. J Med Genet. 2009. PMID: 19181906 Free PMC article.
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: mitchell me. 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.
Renin-angiotensin-aldosterone genotype influences ventricular remodeling in infants with single ventricle.
Mital S, Chung WK, Colan SD, Sleeper LA, Manlhiot C, Arrington CB, Cnota JF, Graham EM, Mitchell ME, Goldmuntz E, Li JS, Levine JC, Lee TM, Margossian R, Hsu DT; Pediatric Heart Network Investigators. Mital S, et al. Among authors: mitchell me. Circulation. 2011 May 31;123(21):2353-62. doi: 10.1161/CIRCULATIONAHA.110.004341. Epub 2011 May 16. Circulation. 2011. PMID: 21576655 Free PMC article. Clinical Trial.
Influence of temperature during transportation on cell-free DNA analysis.
Hidestrand M, Stokowski R, Song K, Oliphant A, Deavers J, Goetsch M, Simpson P, Kuhlman R, Ames M, Mitchell M, Tomita-Mitchell A. Hidestrand M, et al. Fetal Diagn Ther. 2012;31(2):122-8. doi: 10.1159/000335020. Epub 2012 Jan 19. Fetal Diagn Ther. 2012. PMID: 22261730
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: mitchell me. 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.
387 results