Laboratory molecular genetic examination
The laboratory of molecular genetics examines a series of genes, whose mutations are connected prevailingly to fertility and congenital defects.
Their list is shown in the international register of genetic laboratories.
We perform the fast examination of amniotic fluid or of chorio villi with the AmnioPCR method.
At present we are preparing the examination of genes, which participate in the origin of deleterious diseases:
- Screening examination of instability of micro-satellites (MSI) from the tissue of tumours of the digestive tracts.
- Examination of mutation of the genes BRCA1 a BRCA2, which affect the origin of parts of tumours of mamma and ovaries.
- Examination of mutation of the NBS1 gene, causing Nijmegen Breakage Syndrom with characteristic appearance and an increased sensitivity to external influences, which may manifest themselves through tumorous diseases.