Autori: van der Ven Amelie T
| Naslov | Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract (Article) |
| Autori | van der Ven Amelie T ... Bogdanovic Radovan M Stajic Natasa ... (broj koautora 64) |
| Info | JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, (2018), vol. 29 br. 9, str. 2348-2361 |
| 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 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
