AMPLIFY™ Technology Enhances Prenatal Screening for 22q11.2 Microdeletion
Myriad Genetics
APRIL 15, 2024
For example, Driscoll (2001) wrote on the benefits of early 22q detection: Couples can opt to pursue diagnostic testing. Mayo Clinic. Genet Med 3 , 14–18 (2001). Such is the case with the 22q11.2 microdeletion syndrome, a relatively common and potentially serious chromosomal abnormality. J Med Genet 1998; 35 : 789–790.
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