TGFBI Gene Mutation Analysis
Kappa opioid receptor (OPRK1) Genotyping
Lactate Dehydrogenase (LDH), Body Fluid
MSH2 Gene Mutation Analysis (Known Mutations, Duplication/Deletion/Sequencing)
Coronary artery atherosclerosis
Calcium, Random, Urine
Albumin Creatinine Ratio
Gluten, IgE
Maternal Screening, Sequential
Neonatal group B Streptococcus infection
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1p36.3 Microdeletion Syndrome, 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
1p36.3 Microdeletion Syndrome, FISH
Medical Test
CPT
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1p36.3 Microdeletion Syndrome, FISH
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