Glycogen storage disease type I (von Gierke disease)
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
Lamotrigine, Urine
Beta-amyloid Protein Ratio 1-42/1-40 (QUEST AD-Detect™, INNOTEST® B-AMYLOID), Plasma
HLA C Genotype
Group A Streptococcus (Streptococcus pyogenes), Culture
Potassium, Serum
HLA Class I and II typing, Antigen or Genotyping
PML-RARA (Promyelocytic Leukemia/Retinoic Acid Receptor Alpha) Translocation, t(15;17) Analysis
HLA Class I Typing, Antigen or Genotyping
LDS
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Splicing Factor 3b Subunit B1 (SF3B1) 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
Splicing Factor 3b Subunit B1 (SF3B1) Gene Mutation Analysis
Medical Test
Diseases (4)
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Splicing Factor 3b Subunit B1 (SF3B1) Gene Mutation Analysis
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