Sertoli cell tumor and gonadoblastoma in an untreated 29-year-old 46,XY phenotypic male with Frasier syndrome carrying a WT1 IVS9+4C>T mutation-Reference-Cited by-同舟云学术

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Sertoli cell tumor and gonadoblastoma in an untreated 29-year-old 46,XY phenotypic male with Frasier syndrome carrying a WT1 IVS9+4C>T mutation

Published:2012-07-15 Issue:3 Volume:11 Page:361-367
ISSN:1109-3099
Container-title:HORMONES
language:
Short-container-title:HJ

Author:

Kitsiou-Tzeli Sophia,Deligiorgi Maria,Malaktari-Skarantavou Sophia,Vlachopoulos Charalampos,Megremis Spyridon,Fylaktou Irene,Traeger-Synodinos Joanne,Kanaka-Gantenbein Christina,Stefanadis Christodoulos,Kanavakis Emmanuel

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Endocrinology, Diabetes and Metabolism

Cited by 8 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. WT1-related disorders: more than Denys-Drash syndrome;Pediatric Nephrology;2024-02-07

2. Frasier Syndrome: A 15-Year-Old Phenotypically Female Adolescent Presenting with Delayed Puberty and Nephropathy;Children;2023-03-17

3. Systematic Review of Genotype-Phenotype Correlations in Frasier Syndrome;Kidney International Reports;2021-10

4. DENYS–DRASH SYNDROME, FRASIER SYNDROME, AND WAGR SYNDROME ( WT1 ‐RELATED DISORDERS);Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30

5. Long-term outcomes and molecular analysis of a large cohort of patients with 46,XY disorder of sex development due to partial gonadal dysgenesis;Clinical Endocrinology;2018-05-23

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