Polymerase Chaine Reaction (PRC); Microsatellite Markers
Angelman Syndrome; Neonatal Diabetes; Prader-Willi Syndrome; Russell-Silver Syndrome; UPD
Mayo Medical Lab
Other Reference Test
Monday and Wednesday; 2 P.M.
0.5-3 mL Whole Blood
Whole blood collected in an ACD (yellow-top) tube is also acceptable. Complete the Molecular Genetics: Congenital Inherited Disease Patient Info form and submit with specimen. For optimal interpretation of results, 3 specimens are required to perform this test. In addition to child specimen, a blood specimen from both parents is required. Each specimen must have a separate order for Uniparental Disomy (UNIPD / Uniparental Disomy ). Only the proband specimen will be charged.
Room Temp: 96 Hours; Refrigerated: 96 Hours; Frozen: Unacceptable
3 mL Whole Blood
0.5 mL Whole Blood
Submit completed Congentical Inherited Disease Patient Info form with specimen room temp.
Insurance authorization required prior to draw for outpatients. MJ approval is required for inpatients.