Diagnostic Center For Genetic Diseases
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
•CVS
• 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