Projects funded by the NCN
Searching genetic causes of new severe/lethal multidefect congenital syndromes in human fetuses.
2017/27/B/NZ5/02223
Keywords:
dysmorphic features mnogie congenital defect lethal syndrome fetus next generation sequencing - NGS whole exom sequencing - WES
Descriptors:
- NZ5_1: Etiology of human diseases
- NZ5_3: Pathogenesis of human diseases
- NZ2_1: Molecular genetics
Panel:
NZ5 - Human and animal noninfectious diseases: etiology, mechanisms, diagnosis and treatment of diseases, poisonings and injuries (without neurological diseases)
Host institution :
Uniwersytet Medyczny im. Piastów Śląskich we Wrocławiu, Wydział Nauk o Zdrowiu
woj. dolnośląskie
Principal investigator (from the host institution):
Number of co-investigators in the project: 6
Call: OPUS 14 - announced on 2017-09-15
Amount awarded: 1 361 500 PLN
Project start date (Y-m-d): 2018-08-22
Project end date (Y-m-d): 2023-02-21
Project duration:: 54 months (the same as in the proposal)
Project status: Project settled
Project description
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