• Clinical diagnosis of patients with genetic disorders
  • Chromosome analysis
  • Prenatal diagnosis
  • Metabolic screening
  • Molecular diagnosis of genetic disorders (Fra X, micodeletions of Y chromosome, CML for Philadelphia, Duechenne muscle dystrophy, spinal muscle atrophy)
  • Participation in scientific research in cooperation with other departments of the Medical Research Institute
  • Teaching activities include teaching students applying for MSc and PhD in Human Genetics.