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<oembed><version>1.0</version><provider_name>Department of Pediatrics</provider_name><provider_url>https://www.med.unc.edu/pediatrics</provider_url><author_name>Jessi Stark</author_name><author_url>https://www.med.unc.edu/pediatrics/author/jtstark/</author_url><title>Dr. Pandya's Laboratory | Department of Pediatrics</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="YyqkvOdoGw"&gt;&lt;a href="https://www.med.unc.edu/pediatrics/gene/research/dr-pandyas-lab/"&gt;Dr. Pandya&#x2019;s Laboratory&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://www.med.unc.edu/pediatrics/gene/research/dr-pandyas-lab/embed/#?secret=YyqkvOdoGw" width="600" height="338" title="&#x201C;Dr. Pandya&#x2019;s Laboratory&#x201D; &#x2014; Department of Pediatrics" data-secret="YyqkvOdoGw" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script type="text/javascript"&gt;
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</html><description>Dr Pandya has been involved with research on genetic hearing loss for more than two decades, and started her career working on genetic modifiers for hearing loss (HL) in individuals with Waardenburg syndrome. She has successfully established the largest national repository of DNA from deaf individuals in the USA.&#xA0; These samples have been screened to &hellip; Read more</description></oembed>
