Engür, Defne; Aydoğdu, Ayvaz; Tetik, Serap; Dişçigil, Berent; Bozkurt, Gökay; Çakmak, Bilin Çetinkaya; Türkmen, Münevver Kaynak
(Adnan Menderes Üniversitesi Tıp Fakültesi Dergisi, 2012)
The 22q11.2 deletion syndrome is a genetic disorder seen inone out of every 4,000-6000 live births. The effects of the deletion can include a variety of physical findings, such as heart problems, cleft palate, facial ...