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Genetic Diseases Diagnosis Center

Our genetic diseases diagnosis center provides diagnostic tests and consultancy services in many areas, especially reproductive genetics. Our diagnostic laboratory provides prenatal, postnatal, and preimplantation genetic diagnosis services related to the chromosomal diseases, single gene diseases, and all other genetic conditions. On the other hand, it provides fetal diagnosis tests from maternal blood with the NGS (Next Generation Sequencer) technology, as well as diagnostic service with exome sequencing and heterozygote scanning panels. The following test groups are in our service: 

Preimplantation Genetic Screening (PGS) 

24 sure array CGH; 

Multicolor FISH 

Preimplantation Genetic Diagnosis (PGD)

FISH application for translocation purpose 

24 Sure Plus (microarray for translocation purpose) 

PGD for single gene diseases (thalassemia, cystic fibrosis etc., diagnosis of all single gene diseases with known mutations) 

PGD applications for diseases that require HLA tissue compatibility 

Prenatal diagnostic tests 

  • Amniocentesis 
  • CVS 
  • Cordocentesis 

Postnatal Diagnostic Tests 

  • Cytogenetic, molecular genetics and molecular cytogenetic diagnostic tests 

Non-invasive fetal diagnostic tests from the mother’s blood (NGS: Next Generation Sequencer Based) 

Cancer Genetics (Tests for hematological and sporadic cancers) 

Heterozygote screening tests 

Genetic counseling service

This content was published by the medical editorial board on 22.02.2021 and updated on 27.04.2023.