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Whole exome sequencing is a sensitive cost-effective method of detecting mutations in osteogenesis imperfecta and Marfan syndrome.

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Whole exome sequencing is a sensitive cost-effective method of detecting mutations in osteogenesis imperfecta and Marfan syndrome. / MCinerney-Leo, A M; Marshall, M S; Gardiner, B; Coucke, P J; Van Laer, L; Loeys, B L; Summers, Kim; Symoens, S; West, J A; West, M J ; Wordsworth, B P; Zankl, A; Leo, P J; Brown, M A; Duncan, E L.

In: BoneKEy reports, Vol. 2, 456, 04.12.2013.

Research output: Contribution to journalArticlepeer-review

Harvard

MCinerney-Leo, AM, Marshall, MS, Gardiner, B, Coucke, PJ, Van Laer, L, Loeys, BL, Summers, K, Symoens, S, West, JA, West, MJ, Wordsworth, BP, Zankl, A, Leo, PJ, Brown, MA & Duncan, EL 2013, 'Whole exome sequencing is a sensitive cost-effective method of detecting mutations in osteogenesis imperfecta and Marfan syndrome.', BoneKEy reports, vol. 2, 456. https://doi.org/10.1038/bonekey.2013.190

APA

MCinerney-Leo, A. M., Marshall, M. S., Gardiner, B., Coucke, P. J., Van Laer, L., Loeys, B. L., Summers, K., Symoens, S., West, J. A., West, M. J., Wordsworth, B. P., Zankl, A., Leo, P. J., Brown, M. A., & Duncan, E. L. (2013). Whole exome sequencing is a sensitive cost-effective method of detecting mutations in osteogenesis imperfecta and Marfan syndrome. BoneKEy reports, 2, [456]. https://doi.org/10.1038/bonekey.2013.190

Vancouver

MCinerney-Leo AM, Marshall MS, Gardiner B, Coucke PJ, Van Laer L, Loeys BL et al. Whole exome sequencing is a sensitive cost-effective method of detecting mutations in osteogenesis imperfecta and Marfan syndrome. BoneKEy reports. 2013 Dec 4;2. 456. https://doi.org/10.1038/bonekey.2013.190

Author

MCinerney-Leo, A M ; Marshall, M S ; Gardiner, B ; Coucke, P J ; Van Laer, L ; Loeys, B L ; Summers, Kim ; Symoens, S ; West, J A ; West, M J ; Wordsworth, B P ; Zankl, A ; Leo, P J ; Brown, M A ; Duncan, E L. / Whole exome sequencing is a sensitive cost-effective method of detecting mutations in osteogenesis imperfecta and Marfan syndrome. In: BoneKEy reports. 2013 ; Vol. 2.