by Sanger
- Hereditary Hyperferritinemia with cataracts Syndrome (HHCS, exon 1 FTL) (Code 20050)
- Initial study for Hereditary Hemochromatosis (C282Y mutation in HFE gene) (Code 20051)
- Familial Genetic study of a known mutation by Sanger, study of one/two/three mutation/s in one gene (Code 20010, 20020, 20030)
- Full HBB’s gene Sanger study (Code 20052)
