Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12188/22409| Title: | Molecular screening of In2G (c.293-13A/C>G) mutation and detected genotypes among the Macedonian patients with classical form of 21-hydroxylase deficiency | Authors: | Anastasovska, Violeta Kochova, Mirjana |
Issue Date: | 14-Oct-2018 | Journal: | International Journal of Neonatal Screening | Conference: | 11th ISNS European Regional Meeting, Bratislava, Slovakia, October 14-17, 2018, P26 | URI: | http://hdl.handle.net/20.500.12188/22409 |
| Appears in Collections: | Faculty of Medicine: Conference papers |
Files in This Item:
| File | Size | Format | |
|---|---|---|---|
| 11th ISNS - Bratislava, 2018, P26.pdf | 1.16 MB | Adobe PDF | View/Open |
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