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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

Authors

F Stipoljev

stipoljev@yahoo.com

Cytogenetic Laboratory, Department of Obstetrics and Gynecology, Clinical Hospital “Sveti Duh,”, Zagreb, Croatia
Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia

M Barbalic

Genom Ltd, Zagreb, Croatia

M Logara

Genom Ltd, Zagreb, Croatia

A Vicic

Cytogenetic Laboratory, Department of Obstetrics and Gynecology, Clinical Hospital “Sveti Duh,”, Zagreb, Croatia

M Vulic

Department of Gynecology and Obstetrics, Split University Hospital Centre, School of Medicine, University of Split, Split, Croatia

S Zekic Tomas

Pathology Department, University Hospital Centre Split, Split, Croatia
School of Medicine, University of Split, Split, Croatia

R Gjergja Juraski

Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia
Srebrnjak Children’s Hospital, Zagreb, Croatia
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.