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Page 1
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. Among authors: mitchell m. Fetal Diagn Ther. 2012;31(2):122-8. doi: 10.1159/000335020. Epub 2012 Jan 19. Fetal Diagn Ther. 2012. PMID: 22261730
Molecular and cellular basis of congenital heart disease.
Sander TL, Klinkner DB, Tomita-Mitchell A, Mitchell ME. Sander TL, et al. 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.
Fontan palliation in the modern era: factors impacting mortality and morbidity.
Tweddell JS, Nersesian M, Mussatto KA, Nugent M, Simpson P, Mitchell ME, Ghanayem NS, Pelech AN, Marla R, Hoffman GM. Tweddell JS, et al. Among authors: mitchell me. Ann Thorac Surg. 2009 Oct;88(4):1291-9. doi: 10.1016/j.athoracsur.2009.05.076. Ann Thorac Surg. 2009. PMID: 19766824
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.
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
Sparks AB, Wang ET, Struble CA, Barrett W, Stokowski R, McBride C, Zahn J, Lee K, Shen N, Doshi J, Sun M, Garrison J, Sandler J, Hollemon D, Pattee P, Tomita-Mitchell A, Mitchell M, Stuelpnagel J, Song K, Oliphant A. Sparks AB, et al. Among authors: mitchell m. Prenat Diagn. 2012 Jan;32(1):3-9. doi: 10.1002/pd.2922. Epub 2012 Jan 6. Prenat Diagn. 2012. PMID: 22223233 Free PMC article. Clinical Trial.
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.
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18.
Norton ME, Brar H, Weiss J, Karimi A, Laurent LC, Caughey AB, Rodriguez MH, Williams J 3rd, Mitchell ME, Adair CD, Lee H, Jacobsson B, Tomlinson MW, Oepkes D, Hollemon D, Sparks AB, Oliphant A, Song K. Norton ME, et al. Among authors: mitchell me. Am J Obstet Gynecol. 2012 Aug;207(2):137.e1-8. doi: 10.1016/j.ajog.2012.05.021. Epub 2012 Jun 1. Am J Obstet Gynecol. 2012. PMID: 22742782
4,466 results