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S13039-014-0100-9
S13039-014-0100-9
http://dx.doi.org/10.1186/S13039-014-0100-9
Deciphering the pathogenic consequences of chromosomal aberrations in human genetic disease.
P356
Q34987350-0A5F17DC-EF87-4EDF-AE9C-E40572225C50
P356
S13039-014-0100-9
http://dx.doi.org/10.1186/S13039-014-0100-9