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Figure 3 | Orphanet Journal of Rare Diseases

Figure 3

From: Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndrome

Figure 3

FISH results. Two pictures for each reciprocal traslocation of the complex chromosome rearrangement are showed: t(1;13) (A) painting #1 and (B) co-hybridization between the BAC probe RP11-433N2 green (1p31.2) with the probe RB1 red (13q14.2) specific for the retinoblastoma gene; t(3;19) (C) painting #3 and (D) painting #19; t(9;15) (E) painting #9 and (F) probe PWS specific for the Prader-Willi critical region (SNRPN) red (15q11-13), centromeric probe for the chromosome 15 in green and PML in red (15q24.1) as controls; t(14;18) (G) painting #14 and (H) dual color FISH experiment with BACs RP11-151D11 red (18p11p.21) and RP11-138C24 green (18p11.31).

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172