Chronic kidney disease in a child—an unusual crossroad: Answers
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00467-020-04795-x.pdf
Reference14 articles.
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2. Kim S-H, Hu Y, Cadman S, Bouloux P (2007) Diversity in fibroblast growth factor receptor 1 regulation: learning from the investigation of Kallmann syndrome: diversity in fibroblast growth factor receptor 1 regulation. J Neuroendocrinol 20:141–163. https://doi.org/10.1111/j.1365-2826.2007.01627.x
3. Pittock ST, Babovic-Vuksanovic D, Lteif A (2005) Mayer-Rokitansky-Küster-Hauser anomaly and its associated malformations. Am J Med Genet A 135:314–316. https://doi.org/10.1002/ajmg.a.30721
4. Westland R, Schreuder MF, Ket JC, van Wijk JA (2013) Unilateral renal agenesis a systematic review on associated anomalies and renal injury. Nephrol Dial Transplant 28:1844–1855. https://doi.org/10.1093/ndt/gft012
5. Sparnon AL, Ahmed S (1984) Urological anomalies in the caudal regression syndrome. Aust N Z J Surg 54:365–367. https://doi.org/10.1111/j.1445-2197.1984.tb05335.x
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