Interferon-γ Receptor (IFNGR1) Deficiency
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
Saccharomyces cerevisiae Antibody, IgG
Heavy Metals Screen, Random, Urine
Aluminum, 24 Hour, Urine
1,3-Beta-D-Glucan (Fungitell® ß-D Glucan), CSF
Glucose Tolerance Test
Electrophoresis, Protein, 24 Hour, Urine
Aspartoacylase (ASPA) Gene Mutation Analysis (Canavan Disease)
Toxoplasma gondii Antibody, IgE
LDS
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X-linked Intellectual Disability Gene Mutation Panel, NGS
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
X-linked Intellectual Disability Gene Mutation Panel, NGS
Medical Test
Overview
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X-linked Intellectual Disability Gene Mutation Panel, NGS
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