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2 projects found matching your search criteria:

  1. 1. Dissecting the clinical complexity of 22q11 Deletion Syndrome by deep phenotyping and functional genomics.

    Principal investigator: dr hab. Beata Anna Nowakowska

    Instytut Matki i Dziecka

    Call: OPUS 19, Panel: NZ5

  2. 2. Investigation of genetic variants underlying variability in patients with 22q11 Deletion Syndrome.

    Principal investigator: dr Beata Anna Nowakowska

    Instytut Matki i Dziecka

    Call: OPUS 9, Panel: NZ5

Graphic design and implementation: Jakub Piotrowski