A CASE WITH 18q DELETION SYNDROME IDENTIFIED WITH B CELL ABSENCE AND CONGENITAL HEART DISEASE

Guvenc, O.Cimen, D.Kaplan, M. B.Aslan, E.Artac, H.Annagur, A.2020-03-262020-03-2620151015-8146https://hdl.handle.net/20.500.12395/31742[Abstract not Available]eninfo:eu-repo/semantics/closedAccessA CASE WITH 18q DELETION SYNDROME IDENTIFIED WITH B CELL ABSENCE AND CONGENITAL HEART DISEASELetter26445145526852518N/AWOS:000370465300012Q4