Characterisation of genetic variance induced fetal structural anomalies using deep-phenotyping and deep-genotyping

Project Details


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 date1/09/2031/08/21


  • 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


Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.