Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas (Q57667365)
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scientific article published on 25 October 2013
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English | Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas |
scientific article published on 25 October 2013 |
Statements
Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas (English)
Brooke Gardiner
Janelle McFarlane
Mhairi S Marshall
Diana E Benn
25 October 2013
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