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MOLECULAR GENETICS LABORATORY

DISEASE SPECIFIC DNA TESTING

Click on each link to survey the disease specific assays we provide.

Please refer to the Disease Specific DNA Test Order Form to order tests and to review specimen requirements.

Angelman syndrome (methylation analysis)

Beckwith-Wiedemann syndrome

CGH Microarray

Cystic Fibrosis

Fragile X syndrome

Huntington Disease

Hypotonia Panel

Myotonic Dystrophy

Prader-Willi syndrome (methylation analysis)

Russell-Silver syndrome

SNP Microarray

Spinal Muscular Atrophy

Uniparental Disomy (UPD)

Y-deletion



 

 

Contact Information

OUHSC Genetics Laboratory 1122 NE 13th Street, Suite 1400, Oklahoma City, OK 73104

Phone (405)271-3589 Fax (405)271-7117 After hours phone (405)496-9514

   


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