Waardenburg syndrome type 1: a case report of a family with a intragenic PAX3 deletion with no hearing loss or heterochromia of iris.
Abstract
Waardenburg syndrome type 1: a case report of a family with a intragenic PAX3 deletion with no hearing loss or heterochromia of irisCitation
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.Type
ArticleAdditional Links
https://journals.lww.com/clindysmorphol/citation/9900/waardenburg_syndrome_type_1__a_case_report_of_a.65.aspxPMID
38411002Journal
Clinical DysmorphologyPublisher
Lippincott, Williams & Wilkinsae974a485f413a2113503eed53cd6c53
10.1097/MCD.0000000000000482