APA استشهاد

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 شيكاغو

Negishi, Yutaka, et al. "Schaaf-Yang Syndrome Shows a Prader-Willi Syndrome-like Phenotype During Infancy." Orphanet J Rare Dis 2019.

MLA استشهاد

Negishi, 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%.