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Clinical Lab Services

The CLIA-certified ¾Ã¾Ã¾Ã¾Ã¾Ã¾Ã¾Ã¾«Æ· Children's Molecular Diagnostics Lab serves as a pediatric diagnostic center, providing reliable molecular clinical lab services to diagnose more than 30 genetic diseases.

Located at ¾Ã¾Ã¾Ã¾Ã¾Ã¾Ã¾Ã¾«Æ· Children’s Hospital, Delaware, our lab specializes in molecular diagnosis of neuromuscular diseases including muscular dystrophy, spinal muscular atrophy, Emery-Dreifuss muscular dystrophy and Pelizaeus-Merzbacher disease.

Testing is also available for Barth syndrome, Rett syndrome, Pelizaeus-Merzbacher-like disease, Costello syndrome, CFC syndrome, Feingold syndrome and benign hereditary chorea and many others.

• We do not bill third-party payers (insurance companies) for samples received from external sources.
• The person or institution (clinical lab; send-out lab; physician office) sending the sample is responsible for full payment of the invoices within 30 days of receipt of the invoice.
• If a purchase order number is necessary for payment to your institution, please provide it at the time of the sample submission.
• If the patient is on medical assistance, please contact the lab prior to sample submission.
• Invoices are generated when sample tests are completed. We have a 30-day remittance policy from the date of the invoice for receiving payments.
• For direct patient billing, prepayment for the testing services is required prior to beginning our testing. A completedÌýcredit card formÌý (PDF) is required. Please complete the form and include the paperwork with the shipment of the patient sample.

Resources (PDFs)

• CPT Codes and PricingÌý
• Credit Card Authorization Form

Testing Services