1p36.3 Microdeletion Syndrome, FISH
Prenatal Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutation Analysis
Coccidioides Antigen
Blastomyces Antigen, Quantitative, Serum
Anti-Aging Testing Panel
Oncotype DX, Breast Ductal Carcinoma in Situ (DCIS)
HIV-1 Genotypic Protease and Reverse Transcriptase Inhibitor Drug Resistance, Plasma
Oncomine Dx (CDx)
Influenza Virus Type A, B and Respiratory Syncytial Virus (RSV), PCR
LDS
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Hypertrophic Cardiomyopathy Gene Mutation Panel, NGS
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
Hypertrophic Cardiomyopathy Gene Mutation Panel, NGS
Medical Test
Interpretation
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Hypertrophic Cardiomyopathy Gene Mutation Panel, NGS
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