Chromosome Breakage Study, Blood
Wolf-Hirschhorn Syndrome, 4p16.3 Deletion
RET Proto Oncogene Mutation Analysis
Complete Blood Cell Count (CBC) with Differential
Dopamine beta-hydroxylase (DBH) Genetic Variations
Alkaline Phosphatase (ALP), Serum
9p21 Genotype (CVD Risk Genotype Test)
Thioridazine, Urine
Treponema pallidum Antibody, FTA-ABS, IgG, CSF
Chromium, 24 Hour, Urine
LDS
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TGFBR1 Gene Mutation 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
TGFBR1 Gene Mutation Analysis
Medical Test
CPT
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TGFBR1 Gene Mutation Analysis
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