Projects search

• Keywords: arrays CGH ×

Change search criteria ↓

Search results

8 projects found matching your search criteria:

1. 1. Identification of novel structural variants in patients presenting with congenital limb malformations by means of the ge…

   Principal investigator: dr Magdalena Socha

   Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski

   Call: PRELUDIUM 12, Panel: NZ2

2. 2. Identification on novel copy-number variations (CNVs) in patients affected by bilateral congenital limb malformations by…

   Principal investigator: dr hab. Aleksander Marian Jamsheer

   Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski I; Katedra i Zakład Genetyki Medycznej

   Call: SONATA 2, Panel: NZ2

3. 3. Identification of novel genetics variants as the cause of the premature closure of the cranial sutures in children using…

   Principal investigator: Ewelina Maria Bukowska-Olech

   Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski

   Call: PRELUDIUM 12, Panel: NZ5

4. 4. Array-based genomic and transcriptomic profiling in pediatric acute myeloblastic leukemia in search of genes resposible …

   Principal investigator: dr Joanna Szczepanek

   Uniwersytet Mikołaja Kopernika

   Call: SONATA 2, Panel: NZ5

5. 5. Application of array comparative genomic hybridization (aCGH) to identify submicroscopic aberration and lethal genes in …

   Principal investigator: Katarzyna Kowalczyk

   Instytut Matki i Dziecka

   Call: PRELUDIUM 12, Panel: NZ2

6. 6. Identification of novel genetic factors involved in congenital disorders of endocrine gland using advanced methods of ge…

   Principal investigator: dr Bartłomiej Marcin Budny

   Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski II

   Call: SONATA 2, Panel: NZ5

7. 7. Studies on non-coding regulatory copy-number variations as a cause of bilateral limb malformations in humans

   Principal investigator: prof. Aleksander Jamsheer

   Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski

   Call: SONATA BIS 6, Panel: NZ5

8. 8. 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