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The Principles of Clinical Cytogenetics - Extra Materials - Springer

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484 Daynna Wolff and Stuart Schwartz<br />

Fig. 20. Multicolor banding: (A) region-specific probes labeled with different partial chromosome paints<br />

(PCP) and computer false color (MetaSystems’ mBAND) produces a definable number <strong>of</strong> colored bands per<br />

chromosome, regardless <strong>of</strong> chromosome length; (B) this example shows an abnormal X chromosome (right<br />

homolog <strong>of</strong> each pair). Using GTG-banding, the chromosome was initially diagnosed as a paracentric inversion<br />

<strong>of</strong> the long arm (left). mBAND analysis, however, suggests an isodicentric chromosome X (center). Note the<br />

identical band colors in both chromosome arms. An X centromere probe supports this interpretation (right).<br />

(Courtesy <strong>of</strong> MetaSystems Group, Inc.)<br />

Fig. 21. Primed random in situ hybridization (PRINS). Metaphase chromosomes are subjected to PRINS<br />

with α-satellite oligonucleotides specific for chromosomes X, 11, and 17. Bright yellow fluorescein staining is<br />

seen at the centromeres <strong>of</strong> these chromosomes. See text for details. (Courtesy <strong>of</strong> Drs. Steen Kolvraa and Lars<br />

Bolund, Aarhus University, Sweden.)

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