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1755-8166-7-28
1755-8166-7-28
http://dx.doi.org/10.1186/1755-8166-7-28
Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11.
P356
Q33653565-E8A309CE-F86E-49A2-AD2E-76F118CC939B
P356
1755-8166-7-28
http://dx.doi.org/10.1186/1755-8166-7-28