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Detecting mosaic variants in patients with somatic overgrowth syndromes using cell-free circulating DNA and deep sequencing

Authors

  • Wei Shen Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA ARUP Institute for Clinical and Experimental Pathology, ARUP Laboratories, ARUP Laboratories, Salt Lake City, Utah, USA PubMed articlesGoogle scholar articles
  • Josue Flores-Daboub Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA PubMed articlesGoogle scholar articles
  • Dave Viskochil Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA PubMed articlesGoogle scholar articles
  • Sarah L. Dugan Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA PubMed articlesGoogle scholar articles
  • Hunter D. Best Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA ARUP Institute for Clinical and Experimental Pathology, ARUP Laboratories, ARUP Laboratories, Salt Lake City, Utah, USA Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA PubMed articlesGoogle scholar articles
  • Rong Mao Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA ARUP Institute for Clinical and Experimental Pathology, ARUP Laboratories, ARUP Laboratories, Salt Lake City, Utah, USA PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Wei Shen, Pathology, University of Utah School of Medicine, Salt Lake City, UT 84108, USA; shen.wei{at}mayo.edu
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Citation

Shen W, Flores-Daboub J, Viskochil D, et al
Detecting mosaic variants in patients with somatic overgrowth syndromes using cell-free circulating DNA and deep sequencing

Publication history

  • Received November 20, 2019
  • Revised December 30, 2019
  • Accepted January 6, 2020
  • First published January 28, 2020.
Online issue publication 
October 23, 2020

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