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  3. Personalized Genomic Medicine >
  4. Genetic Testing >
  5. Fragile X (FMR1) CGG Repeat Expansion

Personalized Genomic Medicine

  • Darwin OncoTarget™/OncoTreat™
  • Genetic Testing
    • C9orf72 GGGGCC Repeat Expansion
    • Cystic Fibrosis Screening
    • Fragile X (FMR1) CGG Repeat Expansion
    • Huntington Disease (HTT)
    • mtDNA Whole Genome Sequencing
    • Mitochondrial DNA Depletion
    • SNP Oligonucleotide Microarray Analysis (SOMA)
    • Southern Blot for Mitochondrial DNA Rearrangements
    • Spinal Muscular Atrophy – SMN Copy Number
    • Thrombophilia Risk Panel
  • Medical Microbiology Testing
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  • Sohn Precision Medicine Program at Columbia University

Fragile X (FMR1) CGG Repeat Expansion

Purpose: To screen for FMR1 gene mutation (Fragile X).
CPT Codes: 81243
Methodology: Capillary Electrophoresis
Turnaround Time: 14 days
Specimen: Blood
Forms: 1. Requisition Form
2. Informed Consent Form – Carrier Screening
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NewYork-Presbyterian
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