such as Turner, Triple X, Klinefelter and Jacobs syndromes. With the launch of IONA Care+, the comprehensive menu now includes clinically relevant microdeletion syndromes, namely DiGeorge Syndrome ...

A genetic evaluation demonstrated Klinefelter syndrome 47, XXY karyotype with concurrent duplication of 3p21.31 by microarray analysis. Maternal genetic analysis demonstrated the same 3p21.31 ...