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Clinical detection of deletion structural variants in whole-genome sequences.
Noll, Aaron C; Miller, Neil A; Smith, Laurie D; Yoo, Byunggil; Fiedler, Stephanie; Cooley, Linda D; Willig, Laurel K; Petrikin, Josh E; Cakici, Julie; Lesko, John; Newton, Angela; Detherage, Kali; Thiffault, Isabelle; Saunders, Carol J; Farrow, Emily G; Kingsmore, Stephen F.
Afiliação
  • Noll AC; Center for Pediatric Genomic Medicine, Children's Mercy Kansas City, Kansas City, MO, USA.
  • Miller NA; Heartland Institute for Clinical and Translational Research, University of Kansas Medical Center, Kansas City, KS, USA.
  • Smith LD; Department of Pediatrics, Children's Mercy Kansas City, Kansas City, MO, USA.
  • Yoo B; Center for Pediatric Genomic Medicine, Children's Mercy Kansas City, Kansas City, MO, USA.
  • Fiedler S; Center for Pediatric Genomic Medicine, Children's Mercy Kansas City, Kansas City, MO, USA.
  • Cooley LD; Heartland Institute for Clinical and Translational Research, University of Kansas Medical Center, Kansas City, KS, USA.
  • Willig LK; Department of Pediatrics, University of Missouri-Kansas City, Kansas City, MO, USA.
  • Petrikin JE; Center for Pediatric Genomic Medicine, Children's Mercy Kansas City, Kansas City, MO, USA.
  • Cakici J; Department of Pathology, Children's Mercy Kansas City, Kansas City, MO, USA.
  • Lesko J; Department of Pediatrics, University of Missouri-Kansas City, Kansas City, MO, USA.
  • Newton A; Department of Pathology, Children's Mercy Kansas City, Kansas City, MO, USA.
  • Detherage K; Center for Pediatric Genomic Medicine, Children's Mercy Kansas City, Kansas City, MO, USA.
  • Thiffault I; Department of Pediatrics, Children's Mercy Kansas City, Kansas City, MO, USA.
  • Saunders CJ; Department of Pediatrics, University of Missouri-Kansas City, Kansas City, MO, USA.
  • Farrow EG; Center for Pediatric Genomic Medicine, Children's Mercy Kansas City, Kansas City, MO, USA.
  • Kingsmore SF; Department of Pediatrics, Children's Mercy Kansas City, Kansas City, MO, USA.
NPJ Genom Med ; 1: 16026, 2016.
Article em En | MEDLINE | ID: mdl-29263817
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article