WT1: A single gene associated with multiple and severe phenotypes-Reference-Cited by-同舟云学术

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WT1: A single gene associated with multiple and severe phenotypes

Published:2023-12 Issue: Volume:13 Page:100143
ISSN:2666-3961
Container-title:Endocrine and Metabolic Science
language:en
Short-container-title:Endocrine and Metabolic Science

Author:

Ferrari Maria Tereza Martins,Elias Felipe Martins,Gomes Nathalia Lisboa Rosa Almeida,Batista Rafael Loch,Faria José Antonio Diniz,Nishi Mirian Yumie,Mendonca Berenice Bilharinho de,Domenice Sorahia

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference80 articles.

1. Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy;Ahn;Pediatr. Nephrol.,2017

2. WT1 expression in the human fetus during development;Ambu;Eur. J. Histochem.,2015

3. Wilms tumor 1 gene mutations in patients with cytogenetically normal acute myeloid leukemia;Aref;Turk. J. Haematol.,2014

4. Exonic WT1 pathogenic variants in 46,XY DSD associated with gonadoblastoma;Arya;Endocr. Connect.,2021

5. Steroidogenic organ development and homeostasis: a WT1-centric view;Bandiera;Mol. Cell. Endocrinol.,2015

Cited by 1 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. Testicular differentiation in 46,XX DSD: an overview of genetic causes;Frontiers in Endocrinology;2024-04-24

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