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Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants.
Leitsalu, Liis; Alavere, Helene; Jacquemont, Sébastien; Kolk, Anneli; Maillard, Anne M; Reigo, Anu; Nõukas, Margit; Reymond, Alexandre; Männik, Katrin; Ng, Pauline C; Metspalu, Andres.
Afiliação
  • Leitsalu L; Estonian Genome Center, University of Tartu (EGCUT), Tartu, 51010, Estonia.
  • Alavere H; Institute of Molecular & Cell Biology, University of Tartu, Tartu, 51010, Estonia.
  • Jacquemont S; Estonian Genome Center, University of Tartu (EGCUT), Tartu, 51010, Estonia.
  • Kolk A; Service of Medical Genetics, Lausanne University Hospital, Lausanne, 1011, Switzerland.
  • Maillard AM; Estonian Genome Center, University of Tartu (EGCUT), Tartu, 51010, Estonia.
  • Reigo A; Department of Neurology, Children's Clinic of Tartu University Hospital, Tartu, 50406, Estonia.
  • Nõukas M; Service of Medical Genetics, Lausanne University Hospital, Lausanne, 1011, Switzerland.
  • Reymond A; Estonian Genome Center, University of Tartu (EGCUT), Tartu, 51010, Estonia.
  • Männik K; Estonian Genome Center, University of Tartu (EGCUT), Tartu, 51010, Estonia.
  • Ng PC; Institute of Molecular & Cell Biology, University of Tartu, Tartu, 51010, Estonia.
  • Metspalu A; Center for Integrative Genomics, University of Lausanne, Lausanne, 1015, Switzerland.
Per Med ; 13(4): 303-314, 2016 Jul.
Article em En | MEDLINE | ID: mdl-29749813
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Guideline / Qualitative_research / Risk_factors_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

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