Skip to main content
Figure 1 | Molecular Cytogenetics

Figure 1

From: Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up

Figure 1

Patient at 1 year and 10 months (a) and 14 years of age (b) showing the facial dysmorphic features; Partial G-banding karyotype showing paternal balanced translocation (c); Partial FISH metaphase with WCP1 probe showing the patient’s der(11) with the duplicated segment (d); BAC-FISH results showing the breakpoint delineation in 1q32.3 and 11q25 regions in father’s metaphases (e and f); Array result for duplication (blue bar) 1q32.(212,508,954-249,224,376) × 3 (g); and deletion (red bar) 11q25(132,927,027-134,944,770) × 1 (h).

Back to article page

Molecular Cytogenetics

ISSN: 1755-8166