Ziemnicka, K., Budny, B., Drobnik, K., Baszko-Błaszyk, D., Stajgis, M., Katulska, K., . . . Ruchała, M. (2015). Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency. J Appl Genet.
Citação norma ChicagoZiemnicka, K., et al. "Two Coexisting Heterozygous Frameshift Mutations in PROP1 Are Responsible for a Different Phenotype of Combined Pituitary Hormone Deficiency." J Appl Genet 2015.
MLA citiranjeZiemnicka, K., et al. "Two Coexisting Heterozygous Frameshift Mutations in PROP1 Are Responsible for a Different Phenotype of Combined Pituitary Hormone Deficiency." J Appl Genet 2015.
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