Different phenotype with 22q13.3 deletion syndrome in two patients

Gurkan, H.Atli, E.Atli, E.Demir, S.Ozen, Y.Tozkir, H.Eker, D.2024-06-122024-06-1220191018-48131476-5438https://hdl.handle.net/20.500.14551/2618251st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) -- JUN 16-19, 2018 -- Milan, ITALY[Abstract Not Available]eninfo:eu-repo/semantics/closedAccess[No Keywords]Different phenotype with 22q13.3 deletion syndrome in two patientsConference Object27941942Q2WOS:000489313107155