Negishi, Y., Ieda, D., Hori, I., Nozaki, Y., Yamagata, T., Komaki, H., . . . Saitoh, S. (2019). Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy. Orphanet J Rare Dis.
استشهاد بنمط شيكاغوNegishi, Yutaka, et al. "Schaaf-Yang Syndrome Shows a Prader-Willi Syndrome-like Phenotype During Infancy." Orphanet J Rare Dis 2019.
MLA استشهادNegishi, Yutaka, et al. "Schaaf-Yang Syndrome Shows a Prader-Willi Syndrome-like Phenotype During Infancy." Orphanet J Rare Dis 2019.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.