Zobrazeno 1 - 1
of 1
pro vyhledávání: '"22q11 delesyon sendromu"'
Autor:
HAKYEMEZ TOPTAN, Handan, AKBAŞ, Ayşen, GÖKMEN YILDIRIM, Tülin, YAVUZ, Taner, OVALI, Fahri, KARATEKİN, Güner
Publikováno v:
Volume: 46, Issue: 4 118-120
Zeynep Kamil Tıp Bülteni
Zeynep Kamil Tıp Bülteni
Introduction: Classical triad of DiGeorge Syndrome (DGS), where more than %90 of patients are detected by 22q11 deletion, is formed by congenital heart diseases, large vascular anomalies, palatal incapacity, and hypocalcemia. Hypoplasia of timus, spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::d9557c5daa18ef36fc27d6a982bd6629
https://dergipark.org.tr/tr/pub/zktipb/issue/22084/237070
https://dergipark.org.tr/tr/pub/zktipb/issue/22084/237070
