Genetic characterization of a patient with an unusual presentation of Waardenburg syndrome Type 4 and retinoblastoma-Reference-Cited by-同舟云学术

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Genetic characterization of a patient with an unusual presentation of Waardenburg syndrome Type 4 and retinoblastoma

Published:2020-07-16 Issue:1 Volume:68 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Shanthini Thennarasu¹,Balaji Sekaran¹,Kim Usha²,Muthukkaruppan Veerappan³,Vanniarajan Ayyasamy¹^ORCID

Affiliation:

1. Department of Molecular Genetics Aravind Medical Research Foundation Madurai India

2. Department of Orbit Oculoplasty and Oncology Aravind Eye Hospital Madurai India

3. Department of Stem Cell Biology and Immunology Aravind Medical Research Foundation Madurai India

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.28553

Reference9 articles.

1. A Deletion in the Endothelin-B Receptor Gene is Responsible for the Waardenburg Syndrome-Like Phenotypes of WS4 Mice

2. Waardenburg syndrome.

3. Clinical relationship between EDN-3 gene, EDNRB gene and Hirschsprung’s disease

4. Retinoblastoma metastatic to the ovary in a patient with Waardenburg syndrome

5. Interstitial deletion of distal 13q associated with Hirschsprung's disease.

Cited by 2 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. Retinoblastoma and Simulating Lesions;Ocular Pathology;2025

2. Bioinformatics Prediction for Network-Based Integrative Multi-Omics Expression Data Analysis in Hirschsprung Disease;Biomolecules;2024-01-30

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