A rare case of an isolated PAX6 mutation, aniridia, and Wilms tumor-Reference-Cited by-同舟云学术

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A rare case of an isolated PAX6 mutation, aniridia, and Wilms tumor

Published:2020-12-10 Issue:2 Volume:42 Page:216-217
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Lind Katherine T.¹^ORCID,Cost Nicholas G.²,Zegar Kelsey³,Kuldanek Susan A.⁴,Enzenauer Robert W.⁵,Schneider Kami W.¹⁴

Affiliation:

1. Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA

2. Department of Surgery, Division of Urology, University of Colorado School of Medicine, Aurora, CO, USA

3. Genetic Services, InformedDNA, St. Petersburg, FL, USA

4. Center for Cancer and Blood Disorders, Children's Hospital Colorado, Aurora, CO, USA

5. Department of Ophthalmology, Children's Hospital of Colorado, Aurora, CO, USA

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2020.1852577

Reference14 articles.

1. The genetic factors contributing to the development of Wilm's tumor and their clinical utility in its diagnosis and prognosis

2. Epidemiology of Wilms tumor

3. Wilmsʼ tumor

4. Risk Stratification for Wilms Tumor: Current Approach and Future Directions

5. Raised risk of Wilms tumour in patients with aniridia and submicroscopic WT1 deletion

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