Our genetic diseases diagnostic center provides diagnostic tests and consultancy services in many fields including reproductive genesis. With an experience of more than 20 years, it has been offering a high level of genetic service with its modern device park and comprehensive test panel in genetic diagnostics, research and consultancy.
In addition to methods for chromosomal diseases; our diagnostic labs provide prenatal, postnatal and pre-implant genetic diagnosis service for single gene diseases and all other genetic conditions. On the other hand, thanks to NGS (Next Generation Sequencer) technology, it also offers a high level of diagnostic treatment services such as foetal diagnostic tests over mother’s blood, exome sequencing and heterozygote scanning panels. Test groups below are included in our service: 
• Preimplantation genetic scanning (PGS)
• 24 sure array CGH;
• Multi-color FISH 
• Preimplantation genetic diagnosis (PGD)
• FISH implementation for translocation purposes 
• 24 Sure Plus (microarray for translocation purposes)
• PGD for single gen diseases (thalassemia, cystic fibrosis and diagnosis for single gen diseases with known mutation)
• PGD applications for diseases requiring HLA tissue match
• Prenatal diagnostic tests 
• Amniocentesis


• Cordocentesis
• Postnatal diagnostic tests
• Cytogenetic, molecular genetics and molecular cytogenetic diagnostic tests 
• Non-invasive foetal diagnostic tests from mother’s womb (Next Generation Sequencer based)
• Cancer genetic (diagnostic tests for hematologic and sporadic cancers) 
• Heterozygote scanning tests
• Genetic consultancy services