Astrocytoma and Oligodendroglioma
HLA-B27 Genotyping, Ankylosing Spondylitis
Mycoplasma pneumoniae, Culture
Meperidine, Urine
Androgen Receptor (AR) Gene Mutation Analysis
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Branched-chain-ketoacid dehydrogenase (BCKDH) Gene Mutation Analysis
Septin 9 (SEPT9) Methylation Analysis (Epi proColon, ColoVantage)
Haemophilus ducreyi, Culture
Oncotype DX, Prostate Cancer
LDS
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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
Additional ICD10
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15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
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