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Fetal cystic hygroma associated with terminal 2p25.1 duplication and terminal 3p25.3 deletion: Cytogenetic, fluorescent in situ hybridization and microarray familial characterization of two different chromosomal structural rearrangements Cover

Fetal cystic hygroma associated with terminal 2p25.1 duplication and terminal 3p25.3 deletion: Cytogenetic, fluorescent in situ hybridization and microarray familial characterization of two different chromosomal structural rearrangements

Open Access
|Mar 2021

Figures & Tables

Figure 1

(A) Partial karyotype with accompanied ideograms showing balanced translocation (2;3)(p25.1;p25.3) and paracentric inversion of chromosome 3 in the father. (B) Metaphase FISH on paternal peripheral blood lymphocytes using whole-chromosome painting probe for chromosome 3 (green label) and chromosome 3 specific centromere probe (red label). The arrow indicates derivative chromosome 2p resulting from 2p;3p reciprocal translocation. (C) Array comprehensive genomic hybridization analysis of cultured amniotic fluid cells: detailed view of 2(p25.1-p25.3) gain. (D) The 3(p25.3-p26.3) deletion (image from Cytoreport generated by Cytogenomics software; Agilent Technologies).
Language: English
Page range: 79 - 86
Published on: Mar 23, 2021
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 2021 F Stipoljev, M Barbalic, M Logara, A Vicic, M Vulic, S Zekic Tomas, R Gjergja Juraski, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.