NOP10 Gene Mutation Analysis
Neuron-Specific Enolase (NSE), Serum
Bone Morphogenetic Protein Receptor Type 1A (BMPR1A) Gene Mutation Analysis
Clomipramine, Urine
Biopsy, Gallbladder (Cholecystectomy)
Trypsin-Like Immunoreactivity
Infectious mononucleosis
Fatty Acid Profile, Mitochondrial
West Nile Virus (WNV) Antibody, IgG and IgM, CSF
Neonatal Alloimmune Thrombocytopenia
LDS
Sign up
Log in
LDS
/
Medical Tests
/
Kallmann Syndrome, Xp22.3 Deletion, 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
Kallmann Syndrome, Xp22.3 Deletion, FISH
Medical Test
Methodology
Access to
Kallmann Syndrome, Xp22.3 Deletion, FISH
is restricted.
Sign up now
Loading...