Creatine Disorders Panel, Urine Cryoglobulin, Qualitative with Reflex to IFE Typing and Quantitative IgA, IgG, and IgM Creatine Kinase Isoenzymes Cryoglobulin, Qualitative, with Reflex to Quantitative IgA, IgG, and IgM Creatine Kinase, MB Cryptococcus Antigen, CSF Creatine Kinase, Total, Serum or Plasma Cryptococcus Antigen, Serum Creatine Transporter Deficiency (SLC6A8) Deletion/Duplication Cryptosporidium Antigen by EIA Cystic Fibrosis (CFTR) 165 Pathogenic Variants, Fetal Cytogenomic SNP Microarray Cystic Fibrosis (CFTR) Deletion/Duplication Cytogenomic SNP Microarray – Fetal Cystic Fibrosis (CFTR) Sequencing Cystic Fibrosis (CFTR) Sequencing with Reflex to Deletion/Duplication Cystic Respiratory Culture Cyclic Citrullinated Peptide (CCP) Antibody, IgG Cysticercosis Antibody, IgG by ELISA Cyclin D1, SP4 by Immunohistochemistry
