Çağlayan, A. O., Tüysüz, B., Coşkun, S., Quon, J., Harmanci, A. S., Baranoski, J. F., . . . Günel, M. (2016). A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP. J Hum Genet.
Styl ChicagoÇağlayan, Ahmet Okay, et al. "A Patient With a Novel Homozygous Missense Mutation in FTO and Concomitant Nonsense Mutation in CETP." J Hum Genet 2016.
Citace podle MLAÇağlayan, Ahmet Okay, et al. "A Patient With a Novel Homozygous Missense Mutation in FTO and Concomitant Nonsense Mutation in CETP." J Hum Genet 2016.
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