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Genomic sequencing identifies secondary findings in a cohort of parent study participants.
Thompson, Michelle L; Finnila, Candice R; Bowling, Kevin M; Brothers, Kyle B; Neu, Matthew B; Amaral, Michelle D; Hiatt, Susan M; East, Kelly M; Gray, David E; Lawlor, James M J; Kelley, Whitley V; Lose, Edward J; Rich, Carla A; Simmons, Shirley; Levy, Shawn E; Myers, Richard M; Barsh, Gregory S; Bebin, E Martina; Cooper, Gregory M.
Affiliation
  • Thompson ML; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Finnila CR; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Bowling KM; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Brothers KB; Department of Pediatrics, University of Louisville, Louisville, Kentucky, USA.
  • Neu MB; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Amaral MD; University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Hiatt SM; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • East KM; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Gray DE; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Lawlor JMJ; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Kelley WV; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Lose EJ; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Rich CA; University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Simmons S; Department of Pediatrics, University of Louisville, Louisville, Kentucky, USA.
  • Levy SE; University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Myers RM; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Barsh GS; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Bebin EM; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
  • Cooper GM; University of Alabama at Birmingham, Birmingham, Alabama, USA.
Genet Med ; 20(12): 1635-1643, 2018 12.
Article in En | MEDLINE | ID: mdl-29790872
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Exome / Exome Sequencing / Genetic Diseases, Inborn Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2018 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Exome / Exome Sequencing / Genetic Diseases, Inborn Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2018 Document type: Article Affiliation country: Country of publication: