Is microdeletion 2q11.1q1q11.2 pathogenic for CNV / VOUS, a susceptibility factor or just incidental finding?

We discovered the same microdeletion 2q11.1q11.2 for a fetus presenting with cleft lip/ cardiac malformation/ clinodactyly. It is inherited from a father no yet seen in consultation. Is this...

03 February 2015 3,584 2 View