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  <title>Episode 561 - Jeffrey Whitsett, MD</title>
  <description>Cracking the Code: How Genetics Is Rewriting Neonatal Medicine Dr. Jeffrey Whitsett reflects on five decades in neonatal care, tracing the evolution from limited support for preemies to today’s cutting-edge genetic discoveries. Discover how rare gene mutations like TBX4 are reshaping our understanding of lung development and why collaboration with families is key to the next era of life-saving treatments.  Learn more about pulmonary hypertension trials at&amp;amp;nbsp;www.phaware.global/clinicaltrials. Follow us on social @phaware Engage for a cure:&amp;amp;nbsp;www.phaware.global/donate #phaware #phawareMD&amp;amp;nbsp;Share your story: info@phaware.global  Like, Subscribe and Follow us:  www.phawarepodcast.com. @TBX4_Life&amp;amp;nbsp; </description>
  <author_name>I'm Aware That I'm Rare: the phaware® podcast</author_name>
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