Showing 1 - 3 results of 3 for search 'Jaclyn Kotlarek', query time: 0.02s
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<i>TBX3</i> and <i>EFNA4</i> Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis by Moon Ley Tung, Bharatendu Chandra, Jaclyn Kotlarek, Marcelo Melo, Elizabeth Phillippi, Cristina M. Justice, Anthony Musolf, Simeon A. Boyadijev, Paul A. Romitti, Benjamin Darbro, Hatem El-Shanti
Published 2022-09-01
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P145: Paradigm shift in Occam’s Razor and the need for genotype driven reverse phenotyping in rare diseases with complex phenotypes* by Moon Ley Tung, Bharatendu Chandra, Jaime Nagy, Hatem El-Shanti, John Bernat, Nicole Safina, Amy Calhoun, Georgianne Younger, Kyle Dillahunt, Anna Paulson, Taylor Warner, Hannah Bombei, Jaclyn Kotlarek
Published 2024-01-01
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