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
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23 mar 2021
INFORMAZIONI SU QUESTO ARTICOLO
Categoria dell'articolo: Case report
Pubblicato online: 23 mar 2021
Pagine: 79 - 86
DOI: https://doi.org/10.2478/bjmg-2020-0023
Parole chiave
© 2020 Stipoljev F, Barbalic M, Logara M, Vicic A, Vulic M, Zekic Tomas S, Gjergja Juraski R, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Stipoljev, F
Cytogenetic Laboratory, Department of Obstetrics and Gynecology, Clinical Hospital “Sveti Duh,”Zagreb, Croatia
Faculty of Medicine, Josip Juraj Strossmayer University of OsijekOsijek, Croatia
Barbalic, M
Genom LtdZagreb, Croatia
Logara, M
Genom LtdZagreb, Croatia
Vicic, A
Cytogenetic Laboratory, Department of Obstetrics and Gynecology, Clinical Hospital “Sveti Duh,”Zagreb, Croatia
Vulic, M
Department of Gynecology and Obstetrics, Split University Hospital Centre, School of Medicine, University of SplitSplit, Croatia
Zekic Tomas, S
Pathology Department, University Hospital Centre SplitSplit, Croatia
School of Medicine, University of SplitSplit, Croatia
Gjergja Juraski, R
Faculty of Medicine, Josip Juraj Strossmayer University of OsijekOsijek, Croatia
Srebrnjak Children’s HospitalZagreb, Croatia