Hypertrophic Cardiomyopathy Gene Mutation Panel, NGS
Paroxysmal Nocturnal Hemoglobinuria (PNH) (CD55, CD59), Flow, Blood
Erythropoietin
Anthraxin Skin Test
Crystal Identification, Synovial Fluid
Amino Acids Quantitative by LC-MS/MS, Plasma
Son of Sevenless Homolog 1 (SOS1) Gene Mutation Analysis
Felbamate, Urine
TYMS (Thymidylate Synthetase) Gene Mutation Analysis
Creatinine, Serum
LDS
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Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
Medical Test
Reference Ranges
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Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
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