Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12188/22501| Title: | Early onset of complex seizures as a first sign of 16p11.2 deletion syndrome | Authors: | Shukarova Angelovska, Elena Anastasovska, Violeta Duma, Filip Muaremovska, Ljelja Nestoroska, Dragica Ilieva, Gordana Pesevska, Milica Velkov, Milan |
Issue Date: | 6-Jun-2020 | Publisher: | Springer Nature | Journal: | Journal of Human Genetics | Conference: | 53th European Human Genetics Conference, Virtual. Berlin, Germany, June 6-9, 2020 | URI: | http://hdl.handle.net/20.500.12188/22501 |
| Appears in Collections: | Faculty of Medicine: Conference papers |
Files in This Item:
| File | Size | Format | |
|---|---|---|---|
| 53rd ESHG Virtual - 2020, E-P09.42, Shukarova.pdf | 1.12 MB | Adobe PDF | View/Open |
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