Androgen Receptor (AR) Gene Mutation Analysis
Methlyenetetrahydrofolate reductase (MTHFR) Mutation Analysis
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Branched-chain-ketoacid dehydrogenase (BCKDH) Gene Mutation Analysis
Coagulation Factor XI Activity Assay, Plasma
Triazolam, Urine
Chikungunya Virus Antibody, IgM
Congenital malformation
Prostatitis, chronic
Hypoglycemia
LDS
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15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, 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
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
Medical Test
Additional ICD10
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15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
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