Şimşek-Kiper, Pelin Özlem, et al. “A Rare Case of 2q37 Microdeletion With Albright Hereditary Osteodystrophy-Like Phenotype”. The Turkish Journal of Pediatrics, vol. 53, no. 5, Oct. 2011, pp. 558-60, https://doi.org/10.24953/turkjpediatr.2011.1818.