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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 1
2014 1
2015 2
2020 0
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Page 1
Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.
Farwell KD, Shahmirzadi L, El-Khechen D, Powis Z, Chao EC, Tippin Davis B, Baxter RM, Zeng W, Mroske C, Parra MC, Gandomi SK, Lu I, Li X, Lu H, Lu HM, Salvador D, Ruble D, Lao M, Fischbach S, Wen J, Lee S, Elliott A, Dunlop CL, Tang S. Farwell KD, et al. Among authors: dunlop cl. Genet Med. 2015 Jul;17(7):578-86. doi: 10.1038/gim.2014.154. Epub 2014 Nov 13. Genet Med. 2015. PMID: 25356970 Free article.
Not All Next Generation Sequencing Diagnostics are Created Equal: Understanding the Nuances of Solid Tumor Assay Design for Somatic Mutation Detection.
Gray PN, Dunlop CL, Elliott AM. Gray PN, et al. Among authors: dunlop cl. Cancers (Basel). 2015 Jul 17;7(3):1313-32. doi: 10.3390/cancers7030837. Cancers (Basel). 2015. PMID: 26193321 Free PMC article. Review.
Diagnostic testing by CFTR gene mutation analysis in a large group of Hispanics: novel mutations and assessment of a population-specific mutation spectrum.
Schrijver I, Ramalingam S, Sankaran R, Swanson S, Dunlop CL, Keiles S, Moss RB, Oehlert J, Gardner P, Wassman ER, Kammesheidt A. Schrijver I, et al. Among authors: dunlop cl. J Mol Diagn. 2005 May;7(2):289-99. doi: 10.1016/S1525-1578(10)60557-0. J Mol Diagn. 2005. PMID: 15858154 Free PMC article.