INTERGEN Genetics and Rare Diseases Diagnosis Research & Application Center

In 1999, we started our journey with valuable caring to people, life and science. Since then; We develop patient-specific tests even for a single patient, and participate in diagnosis and treatment development of genetic diseases.

 
In INTERGEN, we do more than 90% of our tests by our own designs in R&D center.
 
Patient and team centered; We work with an internal horizontal hierarchical model and participatory management approach.
 
We always are trying to increase awareness on rare diseases, not only in TURKEY, but also throughout the whole world.
 
We teach everything we know to anyone who wants to learn.
 
WE ARE BUILDING A NEW MODEL FOR HEALTH AND R&D CENTER
FOR MANY YEARS “WITHOUT ACTING AS IF”!
 

 

Our Team

  • Assoc. Prof. Serdar CEYLANER
    MD - Medical Geneticist
    Assoc. Prof. of Medical Genetics
  • Assoc. Prof. Gülay Ceylaner, Ph.D.
    MD - Medical Geneticist
    Assoc. Prof. of Medical Genetics
  • Prof. Haldun UMUDUM
    MD - Pathologist
    Prof. of Pathology
  • Latif Zakir KUTUN
    Company Director
  • Çağla ERKAN
    High Biologist - Medical Director
  • Melike AKBAL ŞAHİN
    Biologist
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Laboratory Methods

  • Tissue Culture
    (Lymphocyte, Amnion, Chorion Villus, Fibroblast...)
  • Cytogenetic
    Chromosome analysis from cytogenetic tissues
  • Fluorescent In Situ Hybridization (FISH)
    (Tissue Culture, Swab, Paraffinized Tissue)
  • Comparative Genomic Hybridization
    (Comparative Genomic Hybridization) (CGH)
  • Array Comparative Genomic Hybridization
    (Array Comparative Genomic Hybridization)
  • SNP Micro-Array
    Copy Number Changes-CNV, Uniparental Dysomy
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Study Areas

  • Clinical Genetics
  • Dysmorphology
  • Rare Diseases
  • Genetic Counseling
  • Maternal Fetal Medicine-Genetic Studies
  • Prenatal Diagnosis
  • Preimplantation Genetic Diagnosis (PGT)
  • Postnatal Diagnosis
  • Clinical Reporting
  • Clinical Interpretation of Reports
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