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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1981 1
1985 1
1987 5
1988 2
1989 2
1990 4
1991 4
1992 6
1993 11
1994 2
1995 10
1996 10
1997 9
1998 17
1999 13
2000 5
2001 17
2002 15
2003 20
2004 13
2005 19
2006 17
2007 26
2008 15
2009 18
2010 19
2011 22
2012 20
2013 23
2014 20
2015 13
2016 19
2017 10
2018 17
2019 30
2020 29
2021 26
2022 27
2023 9
2024 7

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PubMed for id: 181980

500 results

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Page 1
A case of Potter sequence with WT1 mutation.
Yoshino M, Shimabukuro W, Takeichi M, Omura J, Yokota C, Yamamoto J, Nakanishi K, Morisada N, Nozu K, Iijima K, Takahashi Y. Yoshino M, et al. CEN Case Rep. 2023 May;12(2):184-188. doi: 10.1007/s13730-022-00742-x. Epub 2022 Oct 13. CEN Case Rep. 2023. PMID: 36227513 Free PMC article.
Papers presented at the fall 2020 Pediatric Urologic Oncology Work Group of the Societies of Pediatric Urology meetingNeonatal Serum Electrolyte and Proteinuria Screening on 46,XY Ambiguous Genitalia Patients May Allow Early Diagnosis of Denys-Drash Syndrome: A Case Report.
Edwards A, Passoni NM, Collins R, Vidi S, Gattineni J, Baker LA. Edwards A, et al. Urology. 2021 Jul;153:312-316. doi: 10.1016/j.urology.2020.11.035. Epub 2020 Dec 3. Urology. 2021. PMID: 33279611
Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort.
Sun S, Xu L, Bi Y, Wang J, Zhang Z, Tang X, Cao Q, Zhai Y, Chen J, Fang X, Liu J, Fang Y, Xiang T, Qian Y, Wu B, Wang H, Zhou W, Shen J, Dong K, Liu X, Zheng B, Zhang A, Wang X, Wu Y, Ma D, Shen Q, Rao J, Xu H. Sun S, et al. Eur J Med Genet. 2020 Nov;63(11):104047. doi: 10.1016/j.ejmg.2020.104047. Epub 2020 Sep 4. Eur J Med Genet. 2020. PMID: 32891756 Free article.
500 results