Scientific background with text space in blue and red. Closeup on plastic tubes for DNA analysis with PCR.
- Comprehensive Inherited Metabolic Disorders
- Connective Tissue Disorders Panel
- Neonatal & Pediatric Critical Care Patients Panel
- Hereditary Cancer Panel
- Neurodevelopmental Disorders
- MODY
- Pan Cancer Cell free DNA test
- Oncomine Focus Assay
- Oncomine Comprehensive Assay Plus
- Full Comprehensive Cancer Panel
- Monogenic Diabetic Panel
- Comprehensive Neonatal Diabetes Mutation Analysis
- Neuromuscular Panel
- Epilepsy Panel
- Ophthalmology Panel
- Hearing Loss Panel
- Comprehensive Renal Panel
- Sickle Cell
- Apolipoprotein B (APOB)
- Apolipoprotein E (APOE) Genotyping, Alzheimer Disease RiskAPO
- Hereditary Hemochromatosis (HHC)
- Celiac Disease HLA-DQ Genotyping
- Factor XIII (F13A1) V34L Variant
- Methylenetetrahydrofolate Reductase (MTHFR) – C677T
- Methylenetetrahydrofolate Reductase (MTHFR)– A1298C
- Factor V Leiden (F5) R506Q Mutation
- Factor II, Activity (Prothrombin)
- Plasminogen Activator Inhibitor-1, PAI-1 (SERPINE1) Genotyping
- HLAB27
- Cystic fibrosis (CF)
- Jak2
- Hearing Loss (GJB2)
- Hemolytic anemia, G6PD deficient (favism)
- Familial Mediterranean fever
- Beta Thalassemia
- Alpha Thalassemia
- Microdeletion Syndrome
- BRCA1 and BRCA2
- Y Chromosome Microdeletion
- Duchenne muscular dystrophy (DMD)
- Congenital Adrenal Hyperplasia (CAH)
- Beta thalassemia (HBB)
- Alpha thalassemia (HBA)
- Spinal Muscular Atrophy (SMA)
- Huntington Disease (HTT)
- Fragile X syndrome
- Myotonic Dystrophy (DM)
- Friedreich’s Ataxia (FA)
- Spinocerebellar Ataxia (SCA)
- Whole Genome Sequencing (WGS)
- Whole Exome Sequencing (WES)
- Comprehensive Cardiac Panel
- Mitochondrial test (mt DNA and Nuclear DNA)
- Mitochondrial test (mtDNA)