Genetics

Diagnosis of hemolytic anemia associated with pyruvate kinase deficiency (exons 3, 5, 7, 8, 10, 11 of the PKLR gene)

Molecular genetic diagnosis of mitochondrial diseases and Leber's optic atrophy (detection of mitochondrial DNA deletions and duplications and 6 common pathogenic variants)

Study of BRCA1, BRCA2 genes by NGS

Extended diagnostics of pathogenic variants in homologous recombination genes: BRCA1, BRCA2, PALB2,

NIPT extended panel (aneuploidies 13, 18, 21, X, Y + 6 microdeletion syndromes in the fetus; carrier

Genetic Passport "Child Development (12 genes)"

DNA Test "Origin" Female

Nutrition, Sports, Vitamins (32 genes)

Genetic Passport "Diet and Sport (17 genes)"

DNA Test "Origin" Male