Hematology

Algorithms

Eosinophil-Related Disorders Testing Algorithm
Hemochromatosis Testing Algorithm
Hemoglobinopathies Testing Algorithm
Hemolytic Anemias Testing Algorithm
Mast Cell Disorders Testing Algorithm
Von Willebrand Disease Testing Algorithm

Topics

Acute Lymphoblastic Leukemia - ALL
Acute Myeloid Leukemia - AML
Chronic Lymphocytic Leukemia - CLL
Chronic Myeloid Leukemia - CML
Eosinophil-Related Disorders - Eosinophilia
Hemochromatosis
Hemoglobinopathies
Hemolytic Anemias
Hemolytic Disease of the Fetus and Newborn
Hemophilia - Factor VIII or IX Deficiency
Hereditary Thrombophilia - Hypercoagulability
Mature B-Cell Lymphomas
Minimal Residual Disease Testing
Myelodysplastic Syndromes
Myeloproliferative Neoplasms - MPNs
Paroxysmal Nocturnal Hemoglobinuria - PNH
Pregnancy and Prenatal Laboratory Testing
T-Cell and NK-Cell Lymphomas
Thalassemias
Uncommon Factor Deficiencies
Unstable Hemoglobinopathies
Von Willebrand Disease - VWD

Test Fact Sheets

Acute Lymphoblastic Leukemia FISH Panels
Acute Myeloid Leukemia Mutation Panel by Next Generation Sequencing
Alloimmune Hemolytic Disease of the Fetus and Newborn (RhCc, RhEe, RhD, or Kell Antigen Genotyping)
Alpha Thalassemia
Beta Globin (HBB) Sequencing
Chronic Lymphocytic Leukemia Mutation Panel by Next Generation Sequencing
Cobalamin/Propionate/Homocysteine Metabolism-Related Disorders Panel
Factor V Leiden (F5) R506Q Variant
Gamma Globin (HBG1 and HBG2) Sequencing
Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency by DNA
Hemochromatosis (HFE) 3 Variants
Hemoglobin Evaluation Reflexive Cascade
Hemophilia A (F8) Genetic Testing
Hereditary Bone Marrow Failure Panel, Sequencing and Deletion/Duplication
Hereditary Hemolytic Anemia Cascade
Hereditary Hemolytic Anemia Panel, Sequencing
JAK2 (V617F) Mutation by ddPCR
Methylenetetrahydrofolate Reductase (MTHFR) Testing
MYD88 L265P Mutation Detection by PCR, Quantitative
Myeloid Malignancies Mutation and Copy Number Variation Panel by Next Generation Sequencing
Plasminogen Activator Inhibitor-1 (SERPINE1) Genotyping
Platelet Antigen Genotyping Panel
Prothrombin (F2) c.*97G>A (G20210A) Pathogenic Variant
Rapid Acute Myeloid Leukemia Targeted Therapy Mutation Panel
RBC Band 3 Protein Reduction in Hereditary Spherocytosis
Red Blood Cell Antigen Genotyping
TPSAB1 Copy Number Analysis by ddPCR
Von Willebrand Disease (VWF) Sequencing
Whole Genome Sequencing