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

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作者： McInerney-Leo,A.M. ^[1] ; Marshall,M.S. ^[2] ; Gardiner,B. ; Benn,D.E. ; McFarlane,J. ; Robinson,B.G. ; Brown,M.A. ; Leo,P.J. ; Clifton-Bligh,R.J. ; Duncan,E.L.

作者单位： Royal North Shore Hospital, Kolling Institute, Sydney, NSW, Australia, University of Sydney, Sydney ^[1] University of Queensland Diamantina Institute, Translational Research Institute Princess Alexandra ^[2]

发布时间 2014-03-08

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Clinical Endocrinology

2014年80卷1期

25-33页

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

Clinical Endocrinology

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Clinical Endocrinology

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

Clinical Endocrinology

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Clinical Endocrinology

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