Kaymakçi, A., Narter, F., Yazar, A. S., & Yilmaz, M. S. (2012). Congenital central hypoventilation syndrome with hirschsprung’s disease due to PHOX2B gene mutation in a Turkish infant. The Turkish Journal of Pediatrics, 54(5), 519-522. https://turkjpediatr.org/article/view/1679