Benign endometrial hyperplasia
Alveolar Rhabdomyosarcoma (ARMS), 13q14 (FOXO1 or FKHR) Rearrangement, FISH, Tissue
Chronic kidney disease
Pregabalin, Urine
Hemoglobin F (Fetal Hemoglobin)
Metabolic syndrome
Cholesterol, Body Fluid
Thiothixene (Navane), Urine
17-Hydroxyprogesterone, Amniotic fluid
Protein Creatinine Ratio

LDS
Sign up
Log in

LDS
/Medical Tests
/FBN1 (Fibrillin-1) Genetic 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

FBN1 (Fibrillin-1) Genetic Mutation Analysis
Medical Test

Access to FBN1 (Fibrillin-1) Genetic Mutation Analysis is restricted.