Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and PAX2[original query] |
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A common variant of the PAX2 gene is associated with reduced newborn kidney size. Journal of the American Society of Nephrology : JASN 2007 Jun 18 (6): 1915-21. Quinlan Jacklyn, Lemire Mathieu, Hudson Thomas, Qu Huiqi, Benjamin Alice, Roy Anne, Pascuet Elena, Goodyer Meigan, Raju Chandhana, Zhang Zhao, Houghton Fiona, Goodyer Pa |
Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children. Pediatric nephrology (Berlin, Germany) 2019 Apr . Vivante Asaf, Chacham Orna Staretz, Shril Shirlee, Schreiber Ruth, Mane Shrikant M, Pode-Shakked Ben, Soliman Neveen A, Koneth Irene, Schiffer Mario, Anikster Yair, Hildebrandt Friedhe |
Phenotypes and genotypes underlying paradoxical pupillary reaction in children. Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus 2022 6 26 (4): 205-207. Khan Arif |
[Genetic analysis of a patient with Papillorenal syndrome due to variant of PAX2 gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 10 39 (10): 1120-1123. Zhao Xuechao, Zheng Yuting, Liu Ning, Wang Conghui, Zhao Ganye, Zhang Junjun, Kong Xiangdo |
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure. Kidney international reports 2023 10 8 (10): 2126-2135. Yishay Ben-Moshe, Omer Shlomovitz, Danit Atias-Varon, Orly Haskin, Efrat Ben-Shalom, Hadas Shasha Lavsky, Oded Volovelsky, Shrikant Mane, Dror Ben-Ruby, Guy Chowers, Karl Skorecki, Yael Borovitz, Maayan Kagan, Nofar Mor, Yulia Khavkin, Shimrit Tzvi-Behr, Shirley Pollack, Moran Plonsky Toder, Michael Geylis, Aviad Schnapp, Rachel Becker-Cohen, Irith Weissman, Ruth Schreiber, Miriam Davidovits, Yaacov Frishberg, Daniella Magen, Ortal Barel, Asaf Vivan |
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