Ве молиме користете го овој идентификатор да го цитирате или поврзете овој запис:
http://hdl.handle.net/20.500.12188/22417| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kochova, Mirjana | en_US |
| dc.contributor.author | Anastasovska, Violeta | en_US |
| dc.date.accessioned | 2022-08-19T09:45:46Z | - |
| dc.date.available | 2022-08-19T09:45:46Z | - |
| dc.date.issued | 2019-04-17 | - |
| dc.identifier.uri | http://hdl.handle.net/20.500.12188/22417 | - |
| dc.language.iso | en | en_US |
| dc.relation.ispartof | Balkan Journal of Medical Genetics | en_US |
| dc.title | Frequency of detected genotypes in patients with salt-wasting form of 21-hydroxylase deficiency | en_US |
| dc.type | Proceeding article | en_US |
| dc.relation.conference | 13th Balkan Congress of Human Genetics, Edirne, Turkey, April 17-20, 2019, P032 | en_US |
| item.grantfulltext | open | - |
| item.fulltext | With Fulltext | - |
| crisitem.author.dept | Faculty of Medicine | - |
| crisitem.author.dept | Faculty of Medicine | - |
| Appears in Collections: | Faculty of Medicine: Conference papers | |
Files in This Item:
| File | Size | Format | |
|---|---|---|---|
| 13th BCHG - Edrine, 2019, P032.pdf | 1.03 MB | Adobe PDF | View/Open |
Записите во DSpace се заштитени со авторски права, со сите права задржани, освен ако не е поинаку наведено.