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Department of Molecular Biology

The Department of Molecular Biology at AEGEAN Medical. In recent years, molecular biology has been used increasingly frequently for the screening and diagnosis of diseases that are either difficult to diagnose using other methods or are caused by defects in an individual’s genetic material. Special mention should be made of Molecular Microbiology, a field that has gained particular diagnostic value due to the SARS-CoV-2 pandemic. Cytogenetic testing (karyotyping) of peripheral blood and other biological materials is performed. Viruses and microbes are detected and identified in various biological materials. Finally, various mutations and polymorphisms that cause diseases are tested. In this department, tests such as the following are performed:

In the Department of Molecular Biology at AEGEAN Medical.

  • FISH (Fluorescence In Situ Hybridisation)

  • Peripheral Blood Karyotype

  • Chorionic Villus Karyotype

  • Amniotic Fluid Karyotype

  • Miscarriage Tissue Karyotype

  • Tissue Karyotyping

  • Bone Marrow Karyotyping

  • Subtelomeric Chromosome Analysis

  • Molecular Detection of SARS-CoV-2 (COVID-19) via RT-PCR

  • Epstein-Barr Virus (EBV)

  • QF-PCR (Amniotic Fluid-Chorionic Villi)

  • Cytomegalovirus (CMV)

  • Adenovirus Detection

  • Enterovirus (EV) Detection/Typing

  • Rubella Virus Detection

  • Detection and Typing of Human Papillomavirus (HPV)

  • Parvovirus B19 Detection

  • Toxoplasma gondii Detection

  • Herpes Simplex Virus 1-2 (HSV 1-2)

  • Hepatitis B Virus (HBV) Detection/Quantification

  • Hepatitis C (HCV) Detection/Quantification/Genotyping

  • Influenza Virus Detection (Influenza A, B, H1N1)

  • Mycobacterium tuberculosis

  • Mycoplasma pneumoniae (Mycoplasma pneumoniae)

  • Mycoplasmas (Mycoplasma hominis, Ureaplasma urealyticum)

  • Chlamydia trachomatis

  • Chlamydia pneumoniae

  • HLA-B27 (PCR)

  • Cystic Fibrosis (CF) 4 Mutations (ME ΔF508)

  • Cystic Fibrosis (CF) 50 Mutations (ME ΔF508)

  • NON-SYNDROMIC HEARING LOSS (35delG)

  • BETA-THALASSEMIA (PCR)

  • GENETIC THROMBOPHILIA 3 MUTATIONS (ME MTHFR-577)

  • GENETIC THROMBOPHILIA 13 MUTATIONS (ME MTHFR-577 & 1298)

  • FACTOR V-LEIDEN (G1691A)

  • FACTOR V-R2 (H1299R)

  • FACTOR II-PROTHROMBIN (G20210A)

  • FACTOR XIII (V34L)

  • APO B (R3500Q)

  • APO E GENOTYPE (E2/E3/E4)

  • MTHFR (C677T)

  • MTHFR (A1298C)

  • PAI-1 (4G/5G)

  • B-FIBRINOGEN (G455A)

  • ACE MUTATION (I/D)

  • GPIIIa – FIBRINOGEN RECEPTOR (HPA-1)

  • GPIba – F-vW RECEPTOR (HPA-2)

  • GPIa – COLLAGEN RECEPTOR (HPA-5)