Kallmann Syndrome, Xp22.3 Deletion, FISH
Chromosome Analysis, Body Fluid
AIRE gene mutation
Alpha 1 Microglobulin, 24 Hour, Urine
Macroprolactin, Serum
Leukemia/Lymphoma Immunophenotyping by Flow Cytometry, Blood
Rickettsia rickettsii DNA, Real-Time PCR
Shiga Toxin, Molecular
Chromosome Analysis, Products of Conception, or Stillbirth
Parvovirus B19 Antibody, IgM
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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