9569:
Fragile X Syndrome, Molecular Analysis
CPT Code Information Current Value
81243-FMR1 (fragile 1 mental retardation 1) (eg, fragile X mental retardation) gene analysis; evaluation to detect abnormal (eg, expanded) alleles
CPT Code Information Value Prior to 1/01/2013 7:02am
81243-FMR1 (fragile 1 mental retardation 1) (eg, fragile X mental retardation) gene analysis; evaluation to detect abnormal (eg, expanded) alleles
Amniotic Fluid Culture for Genetic Testing
88235-Tissue culture for amniotic fluid (if appropriate)
88240-Cryopreservation (if appropriate)
Fibroblast Culture for Genetic Testing
88233-Tissue culture, skin or solid tissue biopsy (if appropriate)
88240-Cryopreservation (if appropriate)
Maternal Cell Contamination, Molecular Analysis
83900 x 6-Amplification, target, multiplex, first 2 nucleic acid sequences (if appropriate)
83909 x 2-Separation and identification by high-resolution technique (if appropriate)
83912-Interpretation and report (if appropriate)
For nonparticipating payers:
Fragile X Syndrome, Molecular Analysis
83890-Molecular isolation or extraction
83900-Amplification, target, multiplex, first 2 nucleic acid sequences
83909-Separation and identification by high-resolution technique
83912-Interpretation and report
Fragile X, Follow-up Analysis
83892 x 2-Enzymatic digestion
83893 x 2-Dot/slot blot production
83894 x 2-Separation by gel electrophoresis
83896-Nucleic acid probe, each
83897 x 2-Nucleic acid transfer
Amniotic Fluid Culture for Genetic Testing
88235-Tissue culture for amniotic fluid (if appropriate)
88240-Cryopreservation (if appropriate)
Fibroblast Culture for Genetic Testing
88233-Tissue culture, skin, or solid tissue biopsy (if appropriate)
88240-Cryopreservation (if appropriate)
Maternal Cell Contamination, Molecular Analysis
83900 x 6-Amplification, target, multiplex, first 2 nucleic acid sequences (if appropriate)
83909 x 2-Separation and identification by high-resolution technique (if appropriate)
83912-Interpretation and report (if appropriate)


