Intergen Genetics Center in Ankara | Rare Diseases & Genetic Testing - Medical Tour: Find & Compare Hospitals, Clinics & Doctors in Turkey

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Intergen Genetics Center in Ankara | Rare Diseases & Genetic Testing

Leading genetics center in Ankara specializing in rare disease diagnosis, cancer genetics, and comprehensive genetic testing. Over 25 years experience with 5,500+ genetic tests and advanced sequencing technologies.

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Google Rating. 4.5

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Languages Supported

English
Turkish
Azerbaijani

Clinical Excellence

Established in 1999, Intergen Genetics and Rare Diseases Center has been at the forefront of genetic diagnostics and research for over 25 years. The center operates with core principles focused on human health and scientific advancement, developing 90% of their 5,500+ genetic tests through their own R&D infrastructure. With a patient-centered approach, they create custom tests for individual cases and actively participate in diagnosis and treatment development for genetic diseases.

Specialized Genetic Services

The center offers comprehensive genetic testing services including marriage and pregnancy carrier screening, genetic risk assessment packages, infertility genetic testing, cancer genetics, clinical genetic counseling, non-invasive prenatal screening, preimplantation genetic testing, and advanced sequencing technologies. Their portfolio includes whole exome sequencing, whole genome sequencing, RNA sequencing, and tumor mutation burden panels.

Research and Education

Intergen maintains strong research credentials with over 100 scientific projects, 250+ international publications, and innovation awards. The center provides educational workshops, scientific project consulting, and thesis guidance, sharing their 25 years of genetic expertise with medical professionals and researchers. They actively support the Rare Disease Volunteers Association to increase awareness and support research in rare diseases and cancer genetics.

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Intergen Genetics Center in Ankara | Rare Diseases & Genetic Testing

Common Questions

Intergen Genetics Center has been operating since 1999 with over 25 years of specialized experience in genetic diagnostics and rare diseases. The center maintains high quality standards through their extensive research background, having developed 90% of their 5,500+ genetic tests through their own R&D infrastructure. While specific international accreditations are not detailed on their website, the center demonstrates quality through their scientific achievements including over 100 research projects, 250+ international publications, and innovation awards. Their clinical genetics team includes 7 specialized doctors led by Prof. Dr. Serdar Ceylaner, all focused on providing accurate genetic diagnostics and counseling. The facility supports the Rare Disease Volunteers Association and maintains active research collaborations, further demonstrating their commitment to quality genetic healthcare.

Intergen Genetics Center provides multilingual support with website content available in English, Turkish, and Azerbaijani, indicating their capacity to serve international patients. The center maintains comprehensive communication channels including email at [email protected], telephone at +90 444-6436, and active social media presence on platforms like LinkedIn, Instagram, Facebook, X (Twitter), YouTube, and TikTok. Located in Ankara's Çankaya district near Bilkent metro station, the facility is easily accessible via public transportation from central areas like Kızılay, AŞTİ, and Sıhhiye. While specific translator services aren't explicitly mentioned, their international publication record and multilingual online presence suggest experience working with diverse patient populations. Patients can communicate through various digital platforms and receive genetic counseling and test results with professional medical interpretation.

The genetic testing process at Intergen Genetics Center begins with comprehensive genetic counseling and clinical examination. Patients can access a wide range of genetic tests including marriage and pregnancy carrier screening (Pregnarisk), genetic risk assessment packages, infertility testing, cancer genetics, non-invasive prenatal screening (NIPT), preimplantation genetic testing (PGT), and advanced sequencing options like whole exome sequencing (WES) and whole genome sequencing (WGS). The center specializes in rare and undiagnosed diseases, often developing custom tests for individual cases. With their extensive R&D capabilities, they design 90% of their tests in-house, ensuring tailored solutions for complex genetic conditions. Test results are typically delivered ahead of schedule, as noted in patient testimonials, and the clinical team provides ongoing support throughout the diagnostic journey. The center handles over 5,500 different genetic tests and maintains a patient-centered approach with continuous communication and follow-up care.

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