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Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations
Naziv: | Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations | Autori: | Hoskins, Bethan E.; Cramer, Carl H.; Tasić, Velibor; Kehinde, Elijah O.; Ashraf, Shazia; Bogdanović, Radovan; Hoefele, Julia; Pohl, Martin; Hildebrandt, Friedhelm | Godina: | 2008 | Publikacija: | Nephrology, dialysis, transplantation | ISSN: | 0931-0509![]() ![]() |
Izdavač: | London : Springer InternationalOxford : Oxford University Press | Tip rezultata: | Ostalo | Kolacija: | vol. 23 br. 2 str. 777-779 | DOI: | 10.1093/ndt/gfm685 | WoS-ID: | 000253022300064 | Scopus-ID: | 2-s2.0-44449157662 | VBS COBISS: | 1025594549 | URI: | https://plus.cobiss.net/cobiss/sr/sr/bib/1025594549#izum.si https://enauka.gov.rs/handle/123456789/668543 |
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