{Reference Type}: Case Reports
{Title}: Waardenburg syndrome type 1: a case report of a family with a intragenic PAX3 deletion with no hearing loss or heterochromia of iris.
{Author}: Macaskill L;Reali L;Naik S;
{Journal}: Clin Dysmorphol
{Volume}: 33
{Issue}: 3
{Year}: 2024 Jul 1
{Factor}: 0.884
{DOI}: 10.1097/MCD.0000000000000482