Waardenburg syndrome: more common than you think!
Author:
Affiliation:
1. Ear, Nose and Throat Department; Doncaster and Bassetlaw NHS Foundation Trust; Doncaster UK
Publisher
Wiley
Subject
Otorhinolaryngology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/coa.12312/fullpdf
Reference11 articles.
1. PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1;Wang;Mol. Vis.,2010
2. Review and update of mutations causing Waardenburg syndrome;Pingault;Hum. Mutat.,2010
3. Different colored eyes. Waardenburg syndrome;Charrow;Pediatr. Ann.,2007
4. Waardenburg syndrome;Read;J. Med. Genet.,1997
5. Delayed presentation of children with Waardenburg syndrome;Mehta;J. Pediatr. Ophthalmol. Strabismus,2010
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1. Comprehensive Approach for the Genetic Diagnosis of Patients with Waardenburg Syndrome;Journal of Personalized Medicine;2024-08-27
2. Cochlear implantation in Waardenburg syndrome: Systematic review and meta-analysis;International Journal of Pediatric Otorhinolaryngology;2023-12
3. A novel variant of the SOX10 gene associated with Waardenburg syndrome type IV;BMC Medical Genomics;2023-06-26
4. Identification of nine novel variants across PAX3 , SOX10 , EDNRB , and MITF genes in Waardenburg syndrome with next‐generation sequencing;Molecular Genetics & Genomic Medicine;2022-11-04
5. A Novel Variant in Paired Box 3 Gene-related with Waardenburg Syndrome Type-1 in an Afghan Family;Journal of the College of Physicians and Surgeons Pakistan;2022-08-01
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