Kallmann Syndrome, Xp22.3 Deletion, FISH
Carcinoembryonic Antigen (CEA), Serum
MSH2 Gene Mutation Analysis (Known Mutations, Duplication/Deletion/Sequencing)
Blastomyces Antibody, Serum
Sulfamethoxazole, Serum
Acetylcholinesterase (AChE), Blood
T Cell Receptor Excision Circles (TREC), Molecular Analysis
Beta-2 Microglobulin, Urine
Secobarbital, Urine
WRAP53 Gene Mutation Analysis
LDS
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Cohen Syndrome Mutation Genetic 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
Cohen Syndrome Mutation Genetic Analysis
Medical Test
LOINC
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Cohen Syndrome Mutation Genetic Analysis
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