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Journal article

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

Publication status:
Published

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Authors


McInerney-Leo, A More by this author
Gardiner, B More by this author
Marshall, M More by this author
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Journal:
JOURNAL OF BONE AND MINERAL RESEARCH
Volume:
28
Publication date:
2013-02-05
ISSN:
0884-0431
URN:
uuid:e28c0159-6094-446f-90e8-e393c0595b66
Source identifiers:
470562
Local pid:
pubs:470562

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