DC Field | Value | Language |
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 |
Appears in Collections: | Cercetări fundamentale
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