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S12887-015-0417-5
S12887-015-0417-5
http://dx.doi.org/10.1186/S12887-015-0417-5
A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
P356
Q35752792-42933682-538A-41C2-9778-C2B141B38CC3
P356
S12887-015-0417-5
http://dx.doi.org/10.1186/S12887-015-0417-5