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. 2016 Sep 14;58(1):93–98. doi: 10.1007/s13353-016-0366-1

Fig. 1.

Fig. 1

The flow-chart showing subsequent detection rates of genomic disorders in patients with the clinical features of 22q11.2 deletion syndrome using various testing approaches (targeted FISH followed by conventional karyotyping, followed by array-CGH)