Salla Disease Mutation Analysis
Splicing Factor 3b Subunit B1 (SF3B1) Gene Mutation Analysis
B and T Cell Gene Rearrangement, Blood
Triiodothyronine (T3), Total
Autoimmune Brain Panel (The Cunningham Panel™ for Autoimmune Neuropsychiatric Disorders)
Biopsy, Endometrial
5-hydroxytryptamine receptor 1A (HTR1A)
ASXL1 Gene Mutation Analysis
CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
BCR-ABL Translocation by RT-PCR, Quantitative, Bone Marrow
LDS
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Hereditary Hemorrhagic Telangiectasia, ENG 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, ENG Gene Mutation Analysis
Medical Test
Additional ICD10
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Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
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