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S11689-016-9150-0
S11689-016-9150-0
http://dx.doi.org/10.1186/S11689-016-9150-0
Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 children.
P356
Q36836952-201098C1-15D0-4487-BCDA-99E04C0D65A8
P356
S11689-016-9150-0
http://dx.doi.org/10.1186/S11689-016-9150-0