The aim of the project is to analyse genetic variances inducing the development of fetus structural anomalies, which is important to obtain knowledge on genetic variances inducing a clear phenotype at the embryonic stage.
|Effective start/end date||1/09/20 → 31/08/21|
- Riga Stradins University: €20,000.00
- Fetal structural anomalies
- next generation sequencing
- deep genotyping
- deep phenotyping
- genetic consultation
- reproductive prognosis
Field of Science
- 3.2 Clinical medicine
Smart Specialization Area
- Biomedicine, medical technologies and biotechnology
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