by Sanger
Genetic studies
by NGS Panels
- Panel for Hereditary Hemochromatosis and Hyper- / Hypoferritinemia (Code 10010)
- Panel for Congenital sideroblastic Anemia and acquired sideroblastic Anaemia (Code 10020)
- Panel for Iron-related Anemia (Code 10030)
- Panel for Congenital dyseritropoietic anemia (Code 10040)
- Panel for Congenital Erythrocytosis / Familial Polycythemia (Code 10050)
- Panel for Hereditary Hemolytic Anemias due to red blood cell enzymopathies or Glycogen storage disease (Code 10061)
- Panel for Hereditary Hemolytic Anemias due to Membranopathies (spherocytosis, elliptocytosis, pyropoycylocytosis, ovalocytosis, stomatocytosis) and Gilbert syndrome as a modifier factor (Code 10062)
- Panel for hereditary hemolytic anemia including membranopathies and enzymopathy (Code 10070)
- Panel for Congenital Erythropoietic Protoporphyria and Congenital erytropoietic Porphyria (Code 10080)
- Panel for Fanconi anemia Code (10090)
- Panel for Diamond-Blackfan Anaemia (Code 10100)
- Panel for dyskeratosis congenita (Code 10110)
- Panel for bone marrow failure (Code 10111)
- Panel for Neurodegeneration with Brain Iron Accumulation Disorders (Code 10120)
