Human Genome Epidemiology Literature Finder
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Query Trace: Frasier Syndrome and WT1[original query] |
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WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes. Pediatric nephrology (Berlin, Germany) 2006 Oct 21 (10): 1393-8. Aucella Filippo, Bisceglia Luigi, De Bonis Patrizia, Gigante Maddalena, Caridi Gianluca, Barbano Giancarlo, Mattioli Gerolamo, Perfumo Francesco, Gesualdo Loreto, Ghiggeri Gian Mar |
Wilms' tumor suppressor gene mutations in girls with sporadic isolated steroid-resistant nephrotic syndrome. Genetics and molecular research : GMR 2013 12 (4): 6184-91. Yang Y H, Zhao F, Feng D N, Wang J J, Wang C F, Huang J, Nie X J, Xia G Z, Chen G M, Yu Z |
Gonadal Function in 15 Patients Associated with WT1 Gene Mutations. Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 2014 5 15 (4): 143-9. Maesaka Akiko, Higuchi Asako, Kotoh Shinobu, Hasegawa Yukihiro, Ikeda Masahiro, Shishido Seiichirou, Honda Masata |
Mutations in WT1 in boys with sporadic isolated steroid-resistant nephrotic syndrome. Genetics and molecular research : GMR 2016 15 (1): . Yang Y, Zhao F, Tu X, Yu |
WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease. Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2021 8 16 (1): 46-54. Ferrari Maria T M, Watanabe Andreia, da Silva Thatiane E, Gomes Nathalia L, Batista Rafael L, Nishi Mirian Y, de Paula Leila C P, Costa Eduardo C, Costa Elaine M F, Cukier Priscilla, Onuchic Luiz F, Mendonca Berenice B, Domenice Sorah |
Genotype-phenotype correlation of WT1 mutation-related nephropathy in Chinese children. Frontiers in pediatrics 2023 8 11 1192021. Huanru Chen, Miao Zhang, Jinai Lin, Jieyi Lu, Fazhan Zhong, Fu Zhong, Xia Gao, Xin Li |
Evaluation of pathogenicity of WT1 intron variants by in vitro splicing analysis. Clinical and experimental nephrology 2024 6 . Seiya Inoue, Atsushi Kondo, Yuta Inoki, Yuta Ichikawa, Yu Tanaka, Chika Ueda, Hideaki Kitakado, Ryota Suzuki, Eri Okada, Nana Sakakibara, Tomoko Horinouchi, Kandai No |
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