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Rare Constitutional and hereditary Diseases, Whole Exome Sequence Analysis, NGS
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
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Pseudocholinesterase, Total, Serum
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
Pseudocholinesterase, Total, Serum
Medical Test
LOINC
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Pseudocholinesterase, Total, Serum
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