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.
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.
Patient Information (Suspected Diagnosis / Medical History)
We’re available to support you in choosing the diagnostic strategy for individual patients and to discuss the results of the analysis.