Cerebrospinal Fluid Glutamine
9p21 Genotype (CVD Risk Genotype Test)
Antibody Identification, Erythrocytes
Peritonitis
Centromere Antibody, IgG
6-Monoacetylmorphine (6-MAM) Confirmation, Urine
Biopsy, Endometrial
Phenobarbital, Confirmation, Urine
CALR (Calreticulin) Gene Mutation Analysis (exon 9 common variants)
Apolipoprotein A-I (APOA1) Gene Analysis
LDS
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Hypochondroplasia (FGFR3) 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
Hypochondroplasia (FGFR3) Gene Mutation Analysis
Medical Test
Clinical Utility
Access to
Hypochondroplasia (FGFR3) Gene Mutation Analysis
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