Genetische Aspekte konnataler Uropathien-Reference-Cited by-同舟云学术

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Genetische Aspekte konnataler Uropathien

Published:2010-11-07 Issue:12 Volume:158 Page:1209-1216
ISSN:0026-9298
Container-title:Monatsschrift Kinderheilkunde
language:de
Short-container-title:Monatsschr Kinderheilkd

Author:

Weber S.

Publisher

Springer Science and Business Media LLC

Subject

Surgery,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00112-010-2245-x.pdf

Reference31 articles.

1. Abdelhak S, Kalatzis V, Heilig R et al (1997) A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family. Nat Genet 15(2):157–164

2. Adalat S, Woolf AS, Johnstone KA et al (2009) HNF1B mutations associate with hypomagnesemia and renal magnesium wasting. J Am Soc Nephrol 20(5):1123–1131

3. Bingham C, Bulman MP, Ellard S et al (2001) Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease. Am J Hum Genet 68(1):219–224

4. Brodbeck S, Englert C (2004) Genetic determination of nephrogenesis: the Pax/Eya/Six gene network. Pediatr Nephrol 19(3):249–255

5. Chevalier RL (2004) Perinatal obstructive nephropathy. Semin Perinatol 28(2):124–131

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Oligohydramnion;Monatsschrift Kinderheilkunde;2010-11-21

2. Prognose konnataler Uropathien;Monatsschrift Kinderheilkunde;2010-11-07

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