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

Project Details

Description

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.
StatusActive
Effective start/end date1/09/2031/08/21

Funding

  • Riga Stradins University: €20,000.00

Field of Science

  • 3.2 Clinical medicine

Smart Specialization Area

  • Biomedicine, medical technologies and biotechnology

Keywords

  • Fetal structural anomalies
  • next generation sequencing
  • deep genotyping
  • deep phenotyping
  • genetic consultation
  • reproductive prognosis