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Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas

✍ Scribed by McInerney-Leo, Aideen M.; Marshall, Mhairi S.; Gardiner, Brooke; Benn, Diana E.; McFarlane, Janelle; Robinson, Bruce G.; Brown, Matthew A.; Leo, Paul J.; Clifton-Bligh, Roderick J.; Duncan, Emma L.


Book ID
127391129
Publisher
John Wiley and Sons
Year
2013
Tongue
English
Weight
89 KB
Volume
80
Category
Article
ISSN
0300-0664

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