CEBPA (CCAAT enhancer binding protein alpha) Gene Mutation Analysis
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

Metastatic colon cancer
Disease