Genetic Analysis of Two Female Patients with Incomplete Denys-Drash Syndrome.-Reference-Cited by-同舟云学术

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Genetic Analysis of Two Female Patients with Incomplete Denys-Drash Syndrome.

Published:2000 Issue:6 Volume:47 Page:683-687
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

OHTA SHOICHIRO¹,OZAWA TETSUO²,SHIRAGA HIROSHI³,FUSE HIDEKI¹

Affiliation:

1. Department of Urology, Faculty of Medicine, Toyama Medical and Pharmaceutical University

2. Department of Clinical Laboratory Medicine, Faculty of Medicine, Toyama Medical and Pharmaceutical University

3. Department of Pediatric Nephrology, Tokyo Women's Medical University

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.jstage.jst.go.jp/article/endocrj1993/47/6/47_6_683/_pdf

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Spectrum of Clinical Manifestations in Children With WT1 Mutation: Case Series and Literature Review;Frontiers in Pediatrics;2022-04-15

2. Detailed clinical manifestations at onset and prognosis of neonatal-onset Denys–Drash syndrome and congenital nephrotic syndrome of the Finnish type;Clinical and Experimental Nephrology;2019-04-08

3. A novel WT1 gene mutation in a patient with Wilms’ tumor and 46, XY gonadal dysgenesis;European Journal of Pediatrics;2011-03-08

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