Autori: Zheng Bixia
| Naslov | Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract (Article) |
| Autori | Zheng Bixia ... Stajic Natasa ... (broj koautora 17) |
| Info | NEPHROLOGY DIALYSIS TRANSPLANTATION, (2022), vol. 37 br. 10, str. 1833-1843 |
| Projekat | Begg Family Foundation; program of China Scholarships Council [201908320472]; Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [442070894]; Health Research Board, Ireland [HPF-206-674]; International Pediatric Research Foundation Early Investigators' Exchange Program; Irish Nephrology Society Specialist Registrar Bursary - Eugen Drewlo Chair for Kidney Research and Innovation at the Schulich School of Medicine & Dentistry at Western University, London, Ontario, Canada; American College of Medical Genetics and Genomics Foundation; National Institutes of Health [T32-DK007726, U54HG006504] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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