LabGenetics offers a catalog of diseases that includes more than 1,000 genetic tests, each of which has been optimized and validated by our professionals in our own facilities.
Depending on each specific condition, and for the diagnosis of hereditary and/or rare diseases, LabGenetics performs various molecular studies: NGS and exome sequencing, full gene sequencing, analysis of common mutations, simultaneous sequencing of multiple genes, expansion analysis, detection of large deletions and duplications by MLPA, carrier screening, and more.
