| DC Field | Value | Language |
|---|
| dc.contributor.author | Sorokina, I. N. | - |
| dc.contributor.author | Vinoglyadova, S. V. | - |
| dc.contributor.author | Rudyh, N. A. | - |
| dc.contributor.author | Bezmenova, I. N. | - |
| dc.contributor.author | Verzilina, I. N. | - |
| dc.contributor.author | Orlova, V. S. | - |
| dc.date.accessioned | 2020-01-27T08:16:58Z | - |
| dc.date.available | 2020-01-27T08:16:58Z | - |
| dc.date.issued | 2019 | - |
| dc.identifier.citation | Hereditary disease epidemiology study as the basis for pharmacotherapy need determination among newborns / I.N. Sorokina [et al.] // Journal of international pharmaceutical research. - 2019. - Vol.46.-P. 248-251. - Refer.: p. 250-251. | ru |
| dc.identifier.uri | http://dspace.bsu.edu.ru/handle/123456789/28204 | - |
| dc.description.abstract | According to the screening data of newborns in the Belgorod region (2006 - 2013) the article determined the frequencies of hereditary metabolic diseases in order to establish the need for pharmacotherapy | ru |
| dc.subject | medicine | ru |
| dc.subject | medical genetics | ru |
| dc.subject | hereditary diseases | ru |
| dc.subject | metabolism | ru |
| dc.subject | screening | ru |
| dc.subject | phenylketonuria | ru |
| dc.subject | cystic fibrosis | ru |
| dc.subject | congenital hypothyroidism | ru |
| dc.subject | Belgorod region | ru |
| dc.subject | 2006-2013 | ru |
| dc.title | Hereditary disease epidemiology study as the basis for pharmacotherapy need determination among newborns | ru |
| dc.type | Article | ru |
| Appears in Collections: | Статьи из периодических изданий и сборников (на иностранных языках) = Articles from periodicals and collections (in foreign languages)
|
