Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Wilms Tumor and NPHS2[original query] |
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Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9. Pediatric research 2006 Feb 59 (2): 325-31. Mucha Bettina, Ozaltin Fatih, Hinkes Bernward G, Hasselbacher Katrin, Ruf Rainer G, Schultheiss Michael, Hangan Daniela, Hoskins Bethan E, Everding Anne Schulze, Bogdanovic Radovan, Seeman Thomas, Hoppe Bernd, Hildebrandt Friedhelm, |
Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome. Pediatric nephrology (Berlin, Germany) 2008 Sep 23 (9): 1455-60. Chernin Gil, Heeringa Saskia F, Gbadegesin Rasheed, Liu Jinhong, Hinkes Bernward G, Vlangos Christopher N, Vega-Warner Virginia, Hildebrandt Friedhe |
Auxiliary genetic analysis in a Chinese adolescent NPH family by single nucleotide polymorphism screening. Molecular medicine reports 2020 1 21 (3): 1115-1124. Tang Chunrong, Zhou Daoyuan, Tan Rongshao, Zhong Xiaoshi, Xiao Xiao, Qin Danping, Liu Yun, Hu Jianguang, Liu Y |
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- Page last updated:Apr 29, 2024
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