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P615: Low rate of clinical follow-up for potential germline variants identified in hematologic malignancies with a next generation sequencing panel

P615: Low rate of clinical follow-up for potential germline variants identified in hematologic malignancies with a next generation sequencing panel

Bibliographic Details
Main Authors: Hannah Wollenzien, Thomas Olson, Kelly Rafferty, Scott Turner, Andrea Ferreira-Gonzalez, Elizabeth Barrie
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Genetics in Medicine Open
Online Access:http://www.sciencedirect.com/science/article/pii/S2949774424006678
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http://www.sciencedirect.com/science/article/pii/S2949774424006678

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