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Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes


Authors: Cate R. Paschal, Miranda P. G. Zalusky, Anita E. Beck, Madelyn A. Gillentine, Jaya Narayanan, Nikhita Damaraju, Joy Goffena, Sophie H. R. Storz, Danny E. Miller

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