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Fig. 2 | Molecular Cytogenetics

Fig. 2

From: Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration

Fig. 2

FISH analysis with Xp/Xq subtelomeric probes on peripheral blood metaphases of female IV2. Panel A shows the Xp deletion, with the red arrow indicating the region where the signal probe is absent. Panel B shows the recombinant X chromosome with two Xq probe signals. The X chromosome centromere is marked with a specific aqua alphoid DNA probe

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