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0471142905.HG0924S79
0471142905.HG0924S79
http://dx.doi.org/10.1002/0471142905.HG0924S79
Analysis and annotation of whole-genome or whole-exome sequencing-derived variants for clinical diagnosis.
P356
Q43590500-F9A65DDC-768D-4844-BD23-04DF900F55DB
P356
0471142905.HG0924S79
http://dx.doi.org/10.1002/0471142905.HG0924S79