Hart, P., Becerik, S., Cogulu, D., Emingil, G., Ozdemir-Ozenen, D., Han, S., . . . Hart, T. (2009). Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta. Clin Genet.
Citação norma ChicagoHart, PS, S. Becerik, D. Cogulu, G. Emingil, D. Ozdemir-Ozenen, ST Han, PP Sulima, E. Firatli, and TC Hart. "Novel FAM83H Mutations in Turkish Families With Autosomal Dominant Hypocalcified Amelogenesis Imperfecta." Clin Genet 2009.
ציטוט MLAHart, PS, et al. "Novel FAM83H Mutations in Turkish Families With Autosomal Dominant Hypocalcified Amelogenesis Imperfecta." Clin Genet 2009.
אזהרה: ציטוטים אלה לעיתים לא מדויקים ב 100%.