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
Macaskill, Laura
Reali, Lisa
Naik, Swati
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2024-02-26
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Waardenburg syndrome type 1: a case report of a family with a intragenic PAX3 deletion with no hearing loss or heterochromia of iris
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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.
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