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.
Chicago Style citaatHart, PS, S. Becerik, D. Cogulu, G. Emingil, D. Ozdemir-Ozenen, ST Han, PP Sulima, E. Firatli, en TC Hart. "Novel FAM83H Mutations in Turkish Families With Autosomal Dominant Hypocalcified Amelogenesis Imperfecta." Clin Genet 2009.
MLA citatieHart, PS, et al. "Novel FAM83H Mutations in Turkish Families With Autosomal Dominant Hypocalcified Amelogenesis Imperfecta." Clin Genet 2009.
Let op: Deze citaties zijn niet altijd 100% accuraat.