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Clinical next generation sequencing reveals an H3F3A gene as a new potential gene candidate for microcephaly associated with severe developmental delay, intellectual disability and growth retardation
| Naziv: | Clinical next generation sequencing reveals an H3F3A gene as a new potential gene candidate for microcephaly associated with severe developmental delay, intellectual disability and growth retardation | Autori: | Maver, Ales; Čuturilo, Goran   ; Ruml-Stojanović, Jelena ; Peterlin, Borut |
Godina: | 2019 | Publikacija: | Balkan journal of medical genetics | ISSN: | 1311-0160 Balkan Journal of Medical Genetics Pretraži identifikator |
Izdavač: | [Warsaw, Poland] : Sciendo | Tip rezultata: | Naučni članak | Kolacija: | vol. 22 br. 2 str. 65-68 | DOI: | 10.2478/bjmg-2019-0028 | WoS-ID: | 000503866600009 | Scopus-ID: | 2-s2.0-85078106428 | PMID: | 31942419 | PMCID: | PMC6956640 | URI: | https://enauka.gov.rs/handle/123456789/543640 | URL: | https://sciendo.com/article/10.2478/bjmg-2019-0028 | Izvor metapodataka: | Migrirano iz RIS podataka | M-kategorija: | 23M23 - Međunarodni časopis kategorije M23 |
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