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Identification of Variants Associated With Rare Hematological Disorder Erythrocytosis Using Targeted Next-Generation Sequencing Analysis.
Kristan, Alesa; Pajic, Tadej; Maver, Ales; Rezen, Tadeja; Kunej, Tanja; Kolic, Rok; Vuga, Andrej; Fink, Martina; Zula, Spela; Podgornik, Helena; Anzej Doma, Sasa; Preloznik Zupan, Irena; Rozman, Damjana; Debeljak, Natasa.
Affiliation
  • Kristan A; Medical Centre for Molecular Biology, Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Pajic T; Department of Hematology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Maver A; Clinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Rezen T; Clinical Biochemistry, Faculty of Medicine, University of Maribor, Maribor, Slovenia.
  • Kunej T; Clinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Kolic R; Centre for Functional Genomics and Bio-Chips, Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Vuga A; Department of Animal Science, Biotechnical Faculty, University of Ljubljana, Ljubljana, Slovenia.
  • Fink M; Kemomed Research and Development, Kemomed Ltd., Ljubljana, Slovenia.
  • Zula S; Kemomed Research and Development, Kemomed Ltd., Ljubljana, Slovenia.
  • Podgornik H; Medical Centre for Molecular Biology, Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Anzej Doma S; Department of Hematology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Preloznik Zupan I; Department of Hematology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Rozman D; Department of Hematology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Debeljak N; Clinical Biochemistry, Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Front Genet ; 12: 689868, 2021.
Article de En | MEDLINE | ID: mdl-34349782
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Diagnostic_studies / Risk_factors_studies Langue: En Journal: Front Genet Année: 2021 Type de document: Article Pays d'affiliation: Slovénie Pays de publication: Suisse
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Diagnostic_studies / Risk_factors_studies Langue: En Journal: Front Genet Année: 2021 Type de document: Article Pays d'affiliation: Slovénie Pays de publication: Suisse