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NRG3373
NRG3373
http://dx.doi.org/10.1038/NRG3373
Phenotypic impact of genomic structural variation: insights from and for human disease.
P356
Q34323221-AFD318C8-F0E9-469D-BDBC-FD6402D544E1
P356
NRG3373
http://dx.doi.org/10.1038/NRG3373