DiGeorge II, (FISH)
On demand
Order number :
CO-F06
DiGeorge II microdeletion
Main indication:
10p14 deletion detection.
Test usage:
Analysis by Fluorescence In Situ Hybridization (FISH) is available for a wide range of microdeletion syndromes. This is a rare genetic syndrome characterized by facial anomalies, congenital heart defects, T-cell immune defects, hypoparathyroid/ hypocalcemia and mental retardation. DGS2 is associated with a partial deletion of the short arm of chromosome 10. Patients with this deletion have many of the same conditions as patients with DGS1 del 22q11.2.
NO related applications
There are no report
You May Also Like
