Diagnostic yield of rare skeletal dysplasia conditions in the radiogenomics era

Overview of attention for article published in BMC Medical Genomics, June 2021

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Whole exome sequencing is an effective tool to identify diagnostic variants in patients with skeletal dysplasia previously unconfirmed genetically. Read more in #BMCMedGenomics: -> https://t.co/zFjweYivRp https://t.co/rXNML7yqMP

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