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ABL Kinase domain mutations
Alpha Thalassemia mutations
Alpha-globin Gene SequencingÂ
ALS C9ORF72 Repeat Expansion
BCR/ABL Quantitative
Beta Globin Gene Deletions
Beta Thalassemia mutations (incl. HbS, HbC, HbE)
Beta-globin DNA Sequencing
Calreticulin, Exon 9 Mutation Analysis
Cystic Fibrosis CBAVD Poly T Mutation
Cystic Fibrosis, common mutations
DNA Extract and Hold
Factor V (F5) Leiden Mutation
FLT3 Mutations, Qualitative
Fragile X
Hemochromatosis, Hereditary
Huntington's Disease Triplet Repeat
IL28B Genotype
Janus kinase 2 Mutation, Qualitative
Maternal Cell Contamination
MGMT Promoter Methylation Assay
MYD88 L265P Mutation Detection by PCR, Qualitative
Myeloid Multigene Panel, Blood
Myeloid Multigene Panel, Non-Blood
NPM1 Exon 12 Mutations, Qualitative
PML-RARA BY PCR, qualitative
PML-RARA BY PCR, quantitative
Prader-Willi/Angelman Syndromes
Prothrombin (20210) mutation
RNA Fusions Heme Panel, Blood
RNA Fusions Heme Panel, Non-Blood
Spinal Muscular Atrophy
UDP Glucuronosyltransferase 1A1
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