1.
Simşek-Kiper PO, Utine GE, Alanay Y, Aktaş D, Alikaşifoğlu M, Boduroğlu K. A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype. Turk J Pediatr. 2011;53(5):558-560. Accessed April 22, 2026. https://turkjpediatr.org/article/view/1818