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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1992 | 1 |
1998 | 1 |
2010 | 1 |
2013 | 1 |
2024 | 0 |
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Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development.
Nat Genet. 1992 May;1(2):144-8. doi: 10.1038/ng0592-144.
Nat Genet. 1992.
PMID: 1302008
WT1 gene mutations in Chinese children with early onset nephrotic syndrome.
Li J, Ding J, Zhao D, Yu Z, Fan Q, Chen Y, Zhang H, Zhong X, Huang J, Yao Y, Xiao H.
Li J, et al.
Pediatr Res. 2010 Aug;68(2):155-8. doi: 10.1203/PDR.0b013e3181e4c9e3.
Pediatr Res. 2010.
PMID: 20442690
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Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
Lipska BS, Iatropoulos P, Maranta R, Caridi G, Ozaltin F, Anarat A, Balat A, Gellermann J, Trautmann A, Erdogan O, Saeed B, Emre S, Bogdanovic R, Azocar M, Balasz-Chmielewska I, Benetti E, Caliskan S, Mir S, Melk A, Ertan P, Baskin E, Jardim H, Davitaia T, Wasilewska A, Drozdz D, Szczepanska M, Jankauskiene A, Higuita LM, Ardissino G, Ozkaya O, Kuzma-Mroczkowska E, Soylemezoglu O, Ranchin B, Medynska A, Tkaczyk M, Peco-Antic A, Akil I, Jarmolinski T, Firszt-Adamczyk A, Dusek J, Simonetti GD, Gok F, Gheissari A, Emma F, Krmar RT, Fischbach M, Printza N, Simkova E, Mele C, Ghiggeri GM, Schaefer F; PodoNet Consortium.
Lipska BS, et al.
Kidney Int. 2013 Jul;84(1):206-13. doi: 10.1038/ki.2013.93. Epub 2013 Mar 20.
Kidney Int. 2013.
PMID: 23515051
Free article.
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Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.
Klamt B, Koziell A, Poulat F, Wieacker P, Scambler P, Berta P, Gessler M.
Klamt B, et al.
Hum Mol Genet. 1998 Apr;7(4):709-14. doi: 10.1093/hmg/7.4.709.
Hum Mol Genet. 1998.
PMID: 9499425
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