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Clinical interpretation of cell-based non-invasive prenatal testing for monogenic disorders including repeat expansion disorders: potentials and pitfalls.
Jeppesen, Line Dahl; Hatt, Lotte; Singh, Ripudaman; Schelde, Palle; Ravn, Katarina; Toft, Christian Liebst; Laursen, Maria Bach; Hedegaard, Jakob; Christensen, Inga Baasch; Nicolaisen, Bolette Hestbek; Andreasen, Lotte; Pedersen, Lars Henning; Vogel, Ida; Lildballe, Dorte Launholt.
Afiliação
  • Jeppesen LD; ARCEDI Biotech, Vejle, Denmark.
  • Hatt L; Center for Fetal Diagnostics, Aarhus University, Aarhus, Denmark.
  • Singh R; ARCEDI Biotech, Vejle, Denmark.
  • Schelde P; ARCEDI Biotech, Vejle, Denmark.
  • Ravn K; ARCEDI Biotech, Vejle, Denmark.
  • Toft CL; ARCEDI Biotech, Vejle, Denmark.
  • Laursen MB; Department of Molecular Diagnostics, Aalborg University Hospital, Aalborg, Denmark.
  • Hedegaard J; Center for Preimplantation Genetic Testing, Aalborg University Hospital, Aalborg, Denmark.
  • Christensen IB; ARCEDI Biotech, Vejle, Denmark.
  • Nicolaisen BH; ARCEDI Biotech, Vejle, Denmark.
  • Andreasen L; ARCEDI Biotech, Vejle, Denmark.
  • Pedersen LH; ARCEDI Biotech, Vejle, Denmark.
  • Vogel I; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
  • Lildballe DL; Department of Gynecology and Obstetrics, Aarhus University Hospital, Aarhus, Denmark.
Front Genet ; 14: 1188472, 2023.
Article em En | MEDLINE | ID: mdl-37829280
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Genet Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Dinamarca
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Genet Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Dinamarca