1p36 deletion (monosomy) syndrome
Metanephrines, Urine
Aortic Dysfunction or Dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome type IV, arterial tortuosity syndrome) Gene Mutation Panel, NGS
Endometrial Stromal Tumors (EST), 7p15 (JAZF1), 6p21.32 (PHF1), 17p13.3 (YWHAE) Rearrangement, FISH, Tissue
Androgen Receptor (AR) Gene Mutation Analysis
Brucella Antibody, IgG and IgM
Albumin, Body Fluid
Thyrotropin Releasing Hormone (TRH)
Reducing Substance, Feces
MGMT (O-6-methylguanine-DNA methyltransferase) Methylation Detection
LDS
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CEBPA (CCAAT enhancer binding protein alpha) 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
CEBPA (CCAAT enhancer binding protein alpha) Gene Mutation Analysis
Medical Test
Interpretation
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CEBPA (CCAAT enhancer binding protein alpha) Gene Mutation Analysis
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