Du, Q., Huynh, L. K., Coskun, F., Molina, E., King, M. A., Raj, P., . . . van Oers, N. S. (2019). FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans. J Clin Invest.
استشهاد بنمط شيكاغوDu, Qiumei, et al. "FOXN1 Compound Heterozygous Mutations Cause Selective Thymic Hypoplasia in Humans." J Clin Invest 2019.
MLA استشهادDu, Qiumei, et al. "FOXN1 Compound Heterozygous Mutations Cause Selective Thymic Hypoplasia in Humans." J Clin Invest 2019.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.