Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome
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| Description | scientific article published on 04 December 2013 |
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author: Emma L. Duncan Aideen M McInerney-Leo Kim M Summers Paul Wordsworth Bart L Loeys Matthew A. Brown |
| Publication date | December 4, 2013 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |