Estriol, Unconjugated, Serum
Cystatin C with Estimated GFR, Serum
Fabry Disease (GLA) Gene Mutation Analysis
Williams Syndrome, 7q11.23 Deletion, FISH, Blood
Leukotriene E4, Urine
Complement Component C4
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutation Analysis
Apolipoprotein A-II (APOA2) Gene Analysis
15q11.2 Duplication, FISH
Gram Stain, Routine

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LDS
/Medical Tests
/1p36.3 Microdeletion Syndrome, FISH

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

1p36.3 Microdeletion Syndrome, FISH
Medical Test

Additional ICD10

Access to 1p36.3 Microdeletion Syndrome, FISH is restricted.