Fig. 1From: 16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up16p13.11 microdeletion/microduplication detected using SNP-array. SNP-array revealed 16p13.11 microdeletion in fetus E2510, E2703, P5107, R2823 and R3676, 16p13.11 microduplication in fetus E2797, E3061, P2758, P3650, P5980, P6436, P8174, R358, R476, R857, R1046, R1460, R2229, R3115, and R3753Back to article page