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P308: A clinical practice guideline for genetic testing in perinatal demise: Enhancing diagnosis through multidisciplinary collaboration by Mackenzie Mosera, Samantha Stover, Caitlin Mann, Karee Morgan, Suné van Wyk, Elise Boos, Chelsea Fechter, Emily Morris, Bryce Schuler
Published 2025-01-01Get full text
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O31: X-linked inheritance results in different sex-specific phenotypes, penetrance, disease course, diagnostic odysseys, and newborn screening sensitivity in Fabry disease by Yutaka Furuta, Natalie Owen, Lisa Bastarache, Chelsea Lauderdale, Laila AI-Shaar, Elvira Ponce, Neena Agrawal, Camille Carter, Karee Morgan, Rizwan Hamid, John Phillips, Rory Tinker
Published 2025-01-01Get full text
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