Yehia, L., Niazi, F., Ni, Y., Ngeow, J., Sankunny, M., Liu, Z., . . . Eng, C. (2015). Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer. Am J Hum Genet.
استشهاد بنمط شيكاغوYehia, Lamis, et al. "Germline Heterozygous Variants in SEC23B Are Associated With Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer." Am J Hum Genet 2015.
MLA استشهادYehia, Lamis, et al. "Germline Heterozygous Variants in SEC23B Are Associated With Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer." Am J Hum Genet 2015.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.