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Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract
| Naziv: | Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract | Autori  : | van, der Ven Amelie T; ...; Bogdanovic, Radovan M; Stajic, Natasa; ...; (broj, koautora 64) | Godina: | 2018 | Publikacija: | JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | ISSN: | 1046-6673 Journal of the American Society of Nephrology Pretraži identifikator |
Tip rezultata: | Naučni članak | Kolacija: | vol. 29 br. 9 str. 2348-2361 | DOI: | 10.1681/ASN.2017121265 | WoS-ID: | 000449014200011 | Scopus-ID: | 2-s2.0-85052570660 | URI: | https://enauka.gov.rs/handle/123456789/818364 | Projekat: | German Research Foundation (DFG) [VE969-7] Health Research Board, Ireland grant [HPF-206-674] International Pediatric Research Foundation Early Investigators' Exchange Program Amgen Irish Nephrology Society Specialist Registrar Bursary National Instit |
Izvor metapodataka: | (Preuzeto iz Nasi u WoS) | M-kategorija: | 21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+ |
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