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s12919-016-0042-9
s12919-016-0042-9
https://scigraph.springernature.com/pub.10.1186/s12919-016-0042-9
Comparing strategies for combined testing of rare and common variants in whole sequence and genome-wide genotype data.
P2888
Q31149266-43128846-AA92-4280-952A-C8CE55142F2D
P2888
s12919-016-0042-9
https://scigraph.springernature.com/pub.10.1186/s12919-016-0042-9