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s12887-015-0417-5
s12887-015-0417-5
https://scigraph.springernature.com/pub.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.
P2888
Q35752792-4EE73F90-58FB-4015-8308-1B5B79BC039D
P2888
s12887-015-0417-5
https://scigraph.springernature.com/pub.10.1186/s12887-015-0417-5