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Figure 1 | Molecular Cytogenetics

Figure 1

From: Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies

Figure 1

Identification and characterization of the 9p abnormality by conventional cytogenetics and FISH analysis. (A) G-banded chromosomes 9 with der(9)(pter→p24.3::p11.2→p23::p23→qter). Ideogram showing the region that is duplicated, p11.2-p23 (blue bar), and inverted (red bar). (B) FISH analysis using WCP 9 and (C) subtelomeric probes 305J7T7 for 9p (green) and LSI 9q34 for 9q (aqua). Arrow indicates terminal deletion of 9p.

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