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Anna H. Bauer, Deepthi Rao, Charles B. Chen
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10.1111/j.1651-2227.2002.tb01650.x · 2002
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10.1016/j.bcmd.2012.01.004 · 2012
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10.1097/md.0000000000008620 · 2017
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10.1186/s40001-014-0051-y · 2014
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10.12998/wjcc.v8.i10.2001 · 2020
No additional external references are available.