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Duncan, E, A McInerney-Leo, P Leo, B Gardiner, M Marshall, P Coucke, B Loeys, et al. 2013. “Whole Exome Sequencing Is a Sensitive and Cost-Effective Means of Detecting Mutations in Patients with Marfan Syndrome and Osteogenesis Imperfecta.” JOURNAL OF BONE AND MINERAL RESEARCH 28.