dc.contributor.author |
Soga, Aliona |
|
dc.date.accessioned |
2020-03-25T14:10:19Z |
|
dc.date.available |
2020-03-25T14:10:19Z |
|
dc.date.issued |
2018 |
|
dc.identifier.citation |
SOGA, Aliona. Screeningul biochimic neonatal ca principala metodă de profilaxie a patologiei ereditare = Neonatal biochemical screening as the main method for the prevention of hereditary pathology. In: Culegere de rezumate ştiinţifice ale studenţilor, rezidenţilor şi tinerilor cercetători. Chișinău: CEP ”Medicina”, 2018, p. 26. ISBN 978-9975-82-103-2. |
en_US |
dc.identifier.isbn |
978-9975-82-103-2 |
|
dc.identifier.uri |
http://repository.usmf.md/handle/20.500.12710/8040 |
|
dc.language.iso |
|
en_US |
dc.publisher |
CEP Medicina |
en_US |
dc.subject |
neonatal screening |
en_US |
dc.subject |
phenylketonuria |
en_US |
dc.subject |
congenital hypothyroidism |
en_US |
dc.title |
Screeningul biochimic neonatal ca principala metodă de profilaxie a patologiei ereditare |
en_US |
dc.title.alternative |
Neonatal biochemical screening as the main method for the prevention of hereditary pathology |
en_US |
dc.type |
|
en_US |