INTERGEN Genetics And Rare Diseases Center

In 1999, our journey started with a deep focus on genetics and rare diseases. Since then; we have improved step by step by focusing on each of our patients as special people and tried to carry out our role in developing the diagnosis and treatment methods for genetic and rare diseases in the best possible way.

We are proud that we
• have more than 22 years of brilliance experience through our unique services to patients and communities and working together as one unified team for recovering health and well-being and showing the real results
• Being among the “Top 10” of the world based on genetic tests’ numbers and varieties;
• Owning more than 5,000 varieties of genetics tests which include testing of around 90% of all rare diseases.
• Serving with more than 120 experienced & professional staff.
• 1st winner of Healthcare Revolution Organization-2018 award of the best innovative health company competition in the US among more than 1000 organizations.
• Dealing with more than 250,000 patients in Cytogenetics and Molecular Genetics laboratories and serving unique and qualified professions.
• Participating in many business councils and conferences all around the world.

Intergen is working with hospitals, clinics, family health teams, academic institutions, pharmaceutical companies, retail pharmacies, device manufacturers, nursing homes, private and governmental customers, and across a range of commercial and academic ventures.

We always try to increase awareness of rare diseases locally and globally and teach all we know to anyone who wishes to learn.

FOR MANY YEARS, CONSTRUCTING A NOVEL MODEL OF HEALTH AND R&D CENTER WAS AND IS OUR ENDEAVOR, AND WE ARE DOING THAT “WITHOUT ACTING AS IF”


Clinical Genetics
Rare Diseases
Preimplantation Genetic Diagnosis (PGT)
Non İnvasive Prenatal Test (NIPT )
Genetic Counseling
Maternal Fetal Medicine-Genetic Studies
Prenatal Diagnosis
Postnatal Diagnosis
Clinical Reporting
WES-CES-WGS-NGS-SANGER Sequencing
Bioinformatic
Clinical Interpretation of Reports
Postmortem Evaluation and Autopsy in Fetus and Newborn
Cancer Genetics
Dysmorphology
Pharmacogenetics and Personal Medicine
Congenital Metabolic Diseases
Skeletal System Diseases and Skeletal Dysplasias
Muscle Diseases-Dystrophies
Deafness and Hearing Disorders
Neurogenic Diseases
Genetic Based Endocrinological Diseases
Tissue Culture
Special Test Design for Diagnostic Studies
Next Generation Sequencing Panel Tests for Differential Diagnosis
Molecular Microbiology
Pathology
Clinical Counseling and Consultation
Test Organizations and Medical Material Transfer