Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.2000.00980.x/fullpdf
Reference31 articles.
1. Precocious breast development: a case of unilateral hyperplasia of the adrenal cortex;Arisaka;European Journal of Pediatrics,1985
2. Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndrome;Baird;Oncogene,1992
3. Donor splice site mutations are responsible for Frasier syndrome;Barbaux;Nature Genetics,1997
4. The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor;Barbosa;Human Mutation,1999
5. Overlapping RNA and DNA binding domains of the WT1 tumor suppressor gene product;Bardeesy;Nucleic Acids Research,1998
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