Diagnostic Lab

The diagnostic lab at Greenwood Genetic Center is named to honor the Center’s co-founder, Harold A. Taylor. The facility is made of three separate, but integrated laboratories: the biochemical lab, the cytogenetic lab and the molecular lab. All three laboratories use technologies to help physicians, patients and their families to better understand a disorder and the available treatments for it. The Greenwood Diagnostic Labs utilize traditional and cutting-edge tools such as next-generation sequencing, multiple array CGH platforms and expanding enzyme analysis testing to provide the most accurate and reliable diagnoses available.

Lab requisitions must accompany all samples, and they should be completed by the referring physician or other healthcare provider. The process of ordering tests has been streamlined with our downloadable requisition forms and test finder. A complete list of test CPT Codes and Prices is also available. The test finder lists over 300 tests and general information for each test including:

  • Methodology
  • Specimen requirements
  • Turnaround time
  • CPT Codes
  • Costs

Laboratory faculty and staff are an invaluable part of GGC’s patient care team. They work closely with clinicians to facilitate testing and support genetic counselors and referring physicians with the information they need to provide answers to their patients.

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Biochemical Lab

Biochemical Lab

The Biochemical Laboratory of the Greenwood Genetic Center provides diagnostic and screening tests for a variety of inherited metabolic disorders including:

● Inborn errors of metabolism
● Lysosomal storage diseases
● Mucolipidoses

Cytogenetics Lab

Cytogenetics Lab

The Cytogenetics Laboratory provides the analysis necessary to detect constitutional chromosomal aberrations and abnormalities related to hematological malignancies. Technologies and analyses at the Cytogenetics lab include:

● High resolution karyotyping
● FISH analysis
● Array CGH

Molecular Lab

Molecular Lab

The Molecular Diagnostic Laboratory offers the latest technologies to diagnose a wide variety of disorders from rare disease to more common conditions including:

● Next-generation sequencing
● Sanger sequencing
● Methylation analysis
● Triplet repeat testing

The molecular lab can also provide prenatal diagnosis for many genetic disorders.

Meet Makayla Gunn

Meet Makayla Gunn

Makayla was diagnosed with Rett Syndrome in April of 2015 at the age of two.   At about 18 months, we noticed she had started some repetitive hand motions, and her pediatrician was a little concerned that she did not have many words.  She had learned some sign language, and was saying ‘mama’ and ‘dada’, but that was it.  Then she suddenly stopped all of that.  At her 2 year old check-up, the pediatrician referred us to BabyNet, ...

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