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{'doi': '10.1038/bonekey.2013.190', 'member_id': '1320', 'member': 'Portico', 'container-title': 'BoneKEy Reports', 'primary-resource': 'http://www.portico.org/Portico/article?article=phx23b2jqt0', 'tld': 'portico.org', 'clearbit-logo': 'https://logo.clearbit.com/portico.org', 'coaccess': [], 'multiple-resolution': [{'url': 'http://triggered.stanford.clockss.org/ServeContent?url=https%3A%2F%2Fbonekey.stanford.clockss.org%2F2013%2Fbonekeyreports_2013_bonekey2013190_fulltext%2Fbonekey2013190.pdf', 'tld': 'clockss.org', 'clearbit-logo': 'https://logo.clearbit.com/clockss.org'}, {'url': 'http://triggered.edina.clockss.org/ServeContent?url=https%3A%2F%2Fbonekey.stanford.clockss.org%2F2013%2Fbonekeyreports_2013_bonekey2013190_fulltext%2Fbonekey2013190.pdf', 'tld': 'clockss.org', 'clearbit-logo': 'https://logo.clearbit.com/clockss.org'}], 'type': 'JOURNAL ARTICLE', 'published_date': '4 December 2013', 'publication': 'BoneKEy Reports', 'supplementary_ids': None, 'title': 'Whole exome sequencing is an efficient, sensitive and specific method of\n mutation detection in osteogenesis imperfecta and Marfan syndrome', 'name': None, 'id': None, 'location': None, 'display_doi': 'https://doi.org/10.1038/bonekey.2013.190', 'grant_info': None, 'editors': None, 'authors': 'Aideen M McInerney-Leo | Mhairi S Marshall | Brooke Gardiner | Paul J Coucke | Lut Van Laer | Bart L Loeys | Kim M Summers | Sofie Symoens | Jennifer A West | Malcolm J West | B Paul Wordsworth | Andreas Zankl | Paul J Leo | Matthew A Brown | Emma L Duncan', 'chairs': None}
https://doi.org/10.1038/bonekey.2013.190
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