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| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2018 | Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract | van, der Ven Amelie T; ...; Bogdanovic, Radovan M; Stajic, Natasa; ...; (broj, koautora 64) | Article | 21a+M21a+ |
| 2021 | Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract | Zheng, Bixia; ...; Stajic, Natasa; ...; (broj, koautora 17) | Article | 21aM21a |