Potter Syndrome: A case study
Author:
Publisher
Heighten Science Publications Corporation
Subject
General Medicine
Link
https://www.forensicscijournal.com/articles/jfsr-aid1007.pdf
Reference12 articles.
1. 1. Boucher C, Sandford R. Autosomal dominant polycystic kidney disease (ADPKD, MIM 173900, PKD1 and PKD2 genes, protein products known as polycystin-1 and polycystin-2). Eur J Hum Genet. 2004; 12: 347-354. Ref.: https://goo.gl/bpYdBp
2. 2. Klaassen I, Neuhaus TJ, Mueller-Wiefel DE, Kemper MJ. Antenatal oligohydramnios of renal origin: long-term outcome. Nephrol Dial Transplant. 2007; 22: 432-439. Ref.: https://goo.gl/5JiLmH
3. 3. Manoj MG, Kakkar S. Potter's Syndrome-a fatal constellation of anomalies. Indian J Med Res. 2014; 139: 648-649. Ref.: https://goo.gl/KmdXXU
4. 4. Eccles MR, Stayner CA. Polycystic kidney disease-where gene dosage counts. F1000Prime Rep. 2014; 6: 24. Ref.: https://goo.gl/5FuqbP
5. 5. Igarashi P, Somlo S. Genetics and pathogenesis of polycystic kidney disease. J Am Soc Nephrol. 2002; 13: 2384-2398. Ref.: https://goo.gl/55tYuA
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