AMPLIFYâ„¢ Technology Enhances Prenatal Screening for 22q11.2 Microdeletion
Myriad Genetics
APRIL 15, 2024
Typically, the way to diagnose 22q prenatally is through chorionic villus sampling or an amniocentesis. For example, Driscoll (2001) wrote on the benefits of early 22q detection: Couples can opt to pursue diagnostic testing. Genet Med   3 , 14–18 (2001). Such is the case with the 22q11.2 deletion syndrome in the SMART study. 
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