Whole Exome Sequencing is a Sensitive and Cost-Effective Means of Detecting Mutations in Patients with Marfan Syndrome and Osteogenesis Imperfecta

Whole Exome Sequencing is a Sensitive and Cost-Effective Means of Detecting Mutations in Patients with Marfan Syndrome and Osteogenesis Imperfecta

Bibliografiset tiedot
Päätekijät: Duncan, E, McInerney-Leo, A, Leo, P, Gardiner, B, Marshall, M, Coucke, P, Loeys, B, West, M, West, J, Wordsworth, P, Zankl, A, Brown, M, van Laer, L
Aineistotyyppi: Journal article
Julkaistu: 2013
Kuvaus
Yhteenveto:

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