Center for Molecular Biology and Genetics



Category Medical Specialty
21-hydroxylase deficiency
Amnio PCR
BRAF mutations
BRCA1 & BRCA2 genes full sequencing
BRCA1 gene full sequencing
BRCA2 gene full sequencing
Breast Cancer Panel (19 genes)
c-KIT Mutations - Exons 9, 11
CHEK2 gene mutations
CMV Quantitative
Detection of Aspergillus
Detection of Brucella (B. melitensis)
Detection of Candida
Detection of Coxsackies
Detection of HCV
Detection of Legionella
Detection of Leismania
Detection of Ureaplasma urealyticum
Detection of Yersinia
Detection of Ατύπων Μυκοβακτηριδίων
DNA extraction
DPYD deficiency for 5-FU toxicity
EML4-ALK rearrangement
ERCC1 gene expression
Fetal sex determination from maternal peripheral blood
Full sequencing of the Cystic Fibrosis gene
Genetic predisposition for Parkinson type 2
HBV Genotyping
HBVm Quantitative
HCV Genotyping
HCV Quantitative
HIV Genotyping
HPV DNA screening
HPV Genotyping
Immunophenotyping for Acute Leukemia
Immunophenotyping for B or T lymphoproliferative disease
Immunophenotyping for B, T and N/K subpopulations
Immunophenotyping for Paroxysmal Nocturnal Hemoglobinuria (PNH)
Immunophenotyping of NK-CELLS
KRAS gene mutations
Large Genomic rearrangements for BRCA1
Large Genomic rearrangements for BRCA2
MEK1 gene mutations
Microsatellite Instability (MSI)
Molecular Analysis for Achondroplasia FGFR3
Molecular Analysis for Hypochondroplasia
Molecular Analysis of 21 Μικροελλειπτικών Συνδρόμων
Molecular Analysis of ABL1 gene
Molecular Analysis of ACE