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Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience.
Valencia CA, Husami A, Holle J, Johnson JA, Qian Y, Mathur A, Wei C, Indugula SR, Zou F, Meng H, Wang L, Li X, Fisher R, Tan T, Hogart Begtrup A, Collins K, Wusik KA, Neilson D, Burrow T, Schorry E, Hopkin R, Keddache M, Harley JB, Kaufman KM, Zhang K. Valencia CA, et al. Front Pediatr. 2015 Aug 3;3:67. doi: 10.3389/fped.2015.00067. eCollection 2015. Front Pediatr. 2015. PMID: 26284228 Free PMC article.
Biparental Inheritance of Mitochondrial DNA in Humans.
Luo S, Valencia CA, Zhang J, Lee NC, Slone J, Gui B, Wang X, Li Z, Dell S, Brown J, Chen SM, Chien YH, Hwu WL, Fan PC, Wong LJ, Atwal PS, Huang T. Luo S, et al. Among authors: valencia ca. Proc Natl Acad Sci U S A. 2018 Dec 18;115(51):13039-13044. doi: 10.1073/pnas.1810946115. Epub 2018 Nov 26. Proc Natl Acad Sci U S A. 2018. PMID: 30478036 Free PMC article.
Reply to Lutz-Bonengel et al.: Biparental mtDNA transmission is unlikely to be the result of nuclear mitochondrial DNA segments.
Luo S, Valencia CA, Zhang J, Lee NC, Slone J, Gui B, Wang X, Li Z, Dell S, Brown J, Chen SM, Chien YH, Hwu WL, Fan PC, Wong LJ, Atwal PS, Huang T. Luo S, et al. Among authors: valencia ca. Proc Natl Acad Sci U S A. 2019 Feb 5;116(6):1823-1824. doi: 10.1073/pnas.1821357116. Epub 2019 Jan 23. Proc Natl Acad Sci U S A. 2019. PMID: 30674682 Free PMC article. No abstract available.
Combined immune deficiency in a patient with a novel NFKB2 mutation.
Lindsley AW, Qian Y, Valencia CA, Shah K, Zhang K, Assa'ad A. Lindsley AW, et al. Among authors: valencia ca. J Clin Immunol. 2014 Nov;34(8):910-5. doi: 10.1007/s10875-014-0095-3. Epub 2014 Sep 10. J Clin Immunol. 2014. PMID: 25205549 Free PMC article.
69 results