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Molecular Testing Services

 

We provide DNA studies for the following disorders:

Angelman syndrome (methylation)

Beckwith-Wiedemann syndrome (methylation)

Chromosomal Microarray Analysis (CGH)

Cystic fibrosis (multiple mutation panel)

Fragile X syndrome

Huntington Disease

Hypotonia Panel

Myotonic Dystrophy

Prader-Willi syndrome (methylation)

Russell-Silver syndrome (methylation)

Sickle cell disease

SNP Array

Spinal Muscular Atrophy

Uniparental Disomy (UPD)

Y-deletion

 

These tests were developed and their performance determined by this laboratory. They have not been cleared or approved by the U.S. Food and Drug Administration (FDA). The FDA has determined that such clearance or approval is not necessary. These assays are intended for clinical use.

Information on this web site is provided for informational purposes only and is not a substitute for professional medical advice. You should not use the information on this web site for diagnosing or treating a medical or health condition. If you have or suspect you have a medical problem, promptly contact your professional healthcare provider.

 



Contact Information
Genetics Laboratory
University of Oklahoma Health Sciences Center
1122 NE 13 Street, Suite 1400, Oklahoma City, OK 73104
Phone: (405) 271-3589 |Fax: (405) 271-7117 Email: Dr. Shibo Li

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