Projects funded by the NCN
Identification on novel copy-number variations (CNVs) in patients affected by bilateral congenital limb malformations by means of high-resolution whole-genome array CGH
2011/03/D/NZ2/06136
Keywords:
clinical genetics medical genetics congenital limb malformations congenital limb defects etiopathogenesis of human genetic disorders molecular cytogenetics brachydactyly syndactyly polydactyly ectrodactyly genetic background
Descriptors:
- NZ5_1: Etiology of human diseases
- NZ5_3: Pathogenesis of human diseases
- NZ2_1: Molecular genetics
Panel:
NZ2 - Genetics, genomics: molecular genetics, genomics, proteomics, bioinformatics, systems biology, genetic epidemiology
Host institution :
Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski I, Katedra i Zakład Genetyki Medycznej
woj. wielkopolskie
Principal investigator (from the host institution):
Number of co-investigators in the project: 3
Call: SONATA 2 - announced on 2011-09-15
Amount awarded: 1 000 000 PLN
Project start date (Y-m-d): 2012-09-12
Project end date (Y-m-d): 2015-09-11
Project duration:: 36 months (the same as in the proposal)
Project status: Project settled