Analysis of variation of single genes by conventional Sanger sequencing, deletion or duplication analysis, or fragment length analysis.
Simultaneous, fast, and effective analysis of all known genes associated with a certain disease.
Molecular genetic characterization of tumor tissue to aid in the selection of the best therapeutic intervention.
Parallel analysis of all coding regions of the genome.
Understand genetic risk factors and plan health care.
Analysis of large deletions and duplications across the whole genome.
A non-invasive prenatal test by Cenata GmbH, which can reliably detect the risk of the chromosomal disorders trisomy 21, trisomy 18, and trisomy 13.
We’re available to support you in choosing the diagnostic strategy for individual patients and to discuss the results of the analysis.
Patient Information (Suspected Diagnosis / Medical History)
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