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The HUGO Journal

Official Journal of the Human Genome Organisation

Fig 3 | Genomic Medicine

Fig 3

From: Molecular cytogenetic characterization of two independent karyotypic anomalies in a patient with severe mental retardation and juvenile idiopathic arthritis

Fig 3

(A) FISH analyses with WCP-X on patient chromosomes indicated that the material deleted from one of the X-chromosomes had not been inserted anywhere else in the genome. (B) FISH analysis with WCP-7. The insertion on der(7q) is denoted by an arrow. (C) FISH analysis with WCP-1. The arrow indicates the der(7) chromosome bearing the inserted material from chromosome 1. (D) FISH analysis with subtelomeric probes TelVysion hybridizing to 7q (red) and 7p (green). The subtelomeric region on der(7), identified by an arrow, has been retained despite the insertion of the region 1p13.2-31.2. [The mixed Telvision probe also yields signals within the subtelomeric region of chromosome 15]

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