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Figure 1 | BMC Medical Genetics

Figure 1

From: Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies

Figure 1

Pictures of the 13 patients with pathogenic CNVs. A. Patient 1 (trisomy 18p); B Patient 6 (william- Beuren syndrome); C Patient 13 (del 6q16.1q21); D Patient 14 (del 22q11.2); E patient 16 (dup 1p35.3 p31.3); F patient 17 (del 8p23.1); G patient 18 (del 7q34q36.2); H patient 20 (del 2q33.1q33.3); I patient 34 (dup 7q11.23); J patient 36 (dup 8q24.3/del 16p13.3); K patient 37 (del 22q11.21); L patient 39 (del 10p15.3p14); M patient 45 (del 17q21.3q21).

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