Amoxapine, Urine
ATM/C11orf65 Gene Variation
Thalassemia and Hemoglobinopathy Evaluation
Leptin
von Willebrand Disease 2N (Subtype Normandy), Genotyping
MLH3 Gene Mutation Analysis
5-Flucytosine
Arylsulfatase A, Leukocytes
Protoporphyrins, Fractionation, Whole Blood
Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene Mutation Analysis
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15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
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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
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
Medical Test
Reference Ranges
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15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
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