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Cell‐free DNA results lead to unexpected diagnosis
dc.contributor.authorSmith, Jessica
dc.contributor.authorKean, Victoria
dc.contributor.authorBianchi, Diana W.
dc.contributor.authorFeldman, Gerald
dc.contributor.authorPetrucelli, Nancie
dc.contributor.authorSimon, Michael
dc.contributor.authorGonik, Bernard
dc.date.accessioned2017-08-01T19:08:49Z
dc.date.available2018-09-04T15:09:23Zen
dc.date.issued2017-08
dc.identifier.citationSmith, Jessica; Kean, Victoria; Bianchi, Diana W.; Feldman, Gerald; Petrucelli, Nancie; Simon, Michael; Gonik, Bernard (2017). "Cell‐free DNA results lead to unexpected diagnosis." Clinical Case Reports 5(8): 1323-1326.
dc.identifier.issn2050-0904
dc.identifier.issn2050-0904
dc.identifier.urihttps://hdl.handle.net/2027.42/137758
dc.publisherWiley Periodicals, Inc.
dc.subject.otherCell‐free DNA
dc.subject.othermetastatic neoplasm
dc.subject.othermultiple monosomies
dc.subject.otherprenatal diagnosis
dc.titleCell‐free DNA results lead to unexpected diagnosis
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelInternal Medicine
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/137758/1/ccr31051_am.pdf
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/137758/2/ccr31051.pdf
dc.identifier.doi10.1002/ccr3.1051
dc.identifier.sourceClinical Case Reports
dc.identifier.citedreferenceAmant, F., M. Verheecke, I. Wlodarska, L. Dehaspe, P. Brady, N. Brison, et al. 2015. Presymptomatic identification of cancers in pregnant women during noninvasive prenatal testing. JAMA Oncol. 1: 814 – 819.
dc.identifier.citedreferenceRink, B. D., and M. E. Norton. 2015. Screening for fetal aneuploidy. Semin. Perinatol. 40: 35 – 43.
dc.identifier.citedreferenceLangmead, B. 2010. Aligning short sequencing reads with Bowtie. Curr Protoc Bioinformatics; Chapter 11:Unit 11.7. https://doi.org/10.1002/0471250953.bi1107s32.
dc.identifier.citedreferenceDharajiya, N. G., A. Namba, I. Horiuchi, S. Miyai, D. Farkas, E. Almasri, et al. 2015. Uterine leiomyoma confounding a noninvasive prenatal test result. Prenat. Diagn. 35: 990 – 993.
dc.identifier.citedreferenceOsborne, C. M., E. Hardisty, P. Devers, K. Kaiser‐Rogers, M. Hayden, W. Goodnight, and N. Vora. 2013. Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease. Prenat. Diagn. 33: 609 – 611.
dc.identifier.citedreferenceVaradhachary, G. R. 2011. Carcinoma of unknown primary: focused evaluation. J. Natl. Compr. Canc. Netw. 9: 1406 – 1412.
dc.identifier.citedreferencePavlidis, N. A. 2002. Coexistence of pregnancy and malignancy. Oncologist 7: 279 – 287.
dc.identifier.citedreferenceLecomte, T., N. Ceze, E. Dorval, and P. Laurent‐Puig. 2010. Circulating free tumor DNA and colorectal cancer. Gastroenterol. Clin. Biol. 34: 662 – 681.
dc.identifier.citedreferenceBianchi, D. W., D. Chudova, A. J. Sehnert, S. Bhatt, K. Murray, T. L. Prosen, et al. 2015. Noninvasive prenatal testing and incidental detection of occult maternal malignancies. JAMA 314: 162 – 169.
dc.identifier.citedreferenceBianchi, D. W. 2015. Prepare for unexpected prenatal test results. Nature 522: 29 – 30.
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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