Publication

Waardenburg syndrome type 1: a case report of a family with a intragenic PAX3 deletion with no hearing loss or heterochromia of iris.

Macaskill, Laura
; 
Reali, Lisa
; 
Naik, Swati
Abstract
Waardenburg syndrome type 1: a case report of a family with a intragenic PAX3 deletion with no hearing loss or heterochromia of iris
MIDER Authors
Macaskill, Laura
Citations
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Date
2024-02-26
Type
Article
Subject
Ophthalmology, Paediatrics
Collections
UHB Ophthalmology
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Citation
Macaskill L, Reali L, Naik S. Waardenburg syndrome type 1: a case report of a family with a intragenic PAX3 deletion with no hearing loss or heterochromia of iris. Clin Dysmorphol. 2024 Jul 1;33(3):125-127. doi: 10.1097/MCD.0000000000000482.
Journal / Source Title
Clinical Dysmorphology
DOI
10.1097/MCD.0000000000000482
URI
http://hdl.handle.net/20.500.14200/3867
PMID
38411002
Publisher
Lippincott, Williams & Wilkins
Publisher’s URL
https://journals.lww.com/clindysmorphol/citation/9900/waardenburg_syndrome_type_1__a_case_report_of_a.65.aspx
Publisher’s statement
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