APA stil citiranja

Katavić, M., Kukuruzović, M., Malenica, M., Seneca, S., & Cvitanović-Šojat, L. (2014). Distinctive phenotype in a girl with Rett syndrome and a novel 25 bp deletion mutation in exon 4 (c.881_905del25, nm_004992.3) of the MECP2 gene: Distinctive phenotype in a girl with Rett syndrome and a novel 25 bp deletion mutation in exon 4 (c.881_905del25, nm_004992.3) of the MECP2 gene. Paediatria Croatica, p. 8.

Chicago stil citiranja

Katavić, Matej, Monika Kukuruzović, Maša Malenica, Sara Seneca, and Ljerka Cvitanović-Šojat. "Distinctive phenotype in a girl with Rett syndrome and a novel 25 bp deletion mutation in exon 4 (c.881_905del25, nm_004992.3) of the MECP2 gene: Distinctive phenotype in a girl with Rett syndrome and a novel 25 bp deletion mutation in exon 4 (c.881_905del25, nm_004992.3) of the MECP2 gene." 2014: 8.

MLA stil citiranja

Katavić, Matej, et al. "Distinctive phenotype in a girl with Rett syndrome and a novel 25 bp deletion mutation in exon 4 (c.881_905del25, nm_004992.3) of the MECP2 gene: Distinctive phenotype in a girl with Rett syndrome and a novel 25 bp deletion mutation in exon 4 (c.881_905del25, nm_004992.3) of the MECP2 gene." 2014: 8.

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