Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1-Reference-Cited by-同舟云学术

Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1

Published:1993-11 Issue:5 Volume:123 Page:673-678
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Coppes Max J.,Huff Vicki,Pelletier Jerry

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference35 articles.

1. Association d'un syndrôme anatomo-pathologique de pseudohermaphroditism masculin, d'une tumeur de Wilms, d'une néphropathie parenchymateuse et d'un mosaïcism XX/XY;Denys;Arch Fr Pediatr,1967

2. A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease;Drash;J Pediatr,1970

3. Comment [in reply to Letter: Edidin DV. Pseudohermaphroditism, glomerulopathy, and Wilms tumor (Drash syndrome);Garfunkel;J Pediatr,1985

4. Alteration of the WT1 gene in patients with Wilms' tumor and genitourinary anomalies;Huff;Am J Hum Genet,1991

5. Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome;Pelletier;Cell,1991

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

2. Case Report: A Pathogenic Missense Variant of WT1 Cosegregates With Proteinuria in a Six-Generation Chinese Family With IgA Nephropathy;Frontiers in Medicine;2022-01-31

3. Congenital nephrotic syndrome;Journal of Perinatology;2021-12

4. Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variant;Pediatric Nephrology;2021-10-04

5. New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome;Medicine;2021-05-14