Gendia is a network established by genetic diagnosis laboratories applying genetic tests throughout the world and has a wide range of test panel. With this formation, it is possible to perform more than 2.000 genetic diagnosis tests. It plays an important role in directing the patients and other family members by performing the analyses with its wide range of test panels.

The diagnosis of genetic diseases is important as it causes a meaningful morbidity and mortality. Diagnosing at postnatal and prenatal stage in the families with such diseases is possible after determining the porters, providing genetic consultancy and bringing out the mutations causing the disease by molecular analyses. In addition to this, today, it’s known that the single gene diseases are caused by mutations in more than 1.500 genes. Mutation scans for different gene zones are available today in various laboratories. However, the majority of the genetic laboratories can only diagnose a very limited amount of genetic diseases and when it comes to confirm the diagnosis with the genetic test, people encounter difficulties in finding a center which is able to perform this test.

With this international network featuring more than 50 genetic laboratories from America, Europe and Australia, it is possible to perform more than 2.000 genetic tests and molecular analyses for more than 500 genes.

Being aware of the difficulties encountered by the patients in genetic diagnosis field, our Center has joined this formation in 2007 and started to provide service for the following genetic tests.

• Moleküler Testler
• Moleküler Testler (only newest)
• Next generation sequencing platforms
• Copy Number Tests
• Screening Panels
• Microarray Testing
• Mitochondrial Tests
• Molecular Tests for Leukemia and Lymphoma)
• Molecular Tests in Tumor Tissue
• Test for Risk Factors
• Uniparental (UPD) Tests
• Pharmacogenetic Tests
• FISH Analysis