Sakaguchi, T., Žigman, T., Petković Ramadža, D., Omerza, L., Pušeljić, S., Ereš Hrvaćanin, Z. ... Barić, I. (2018). A Novel PGAP3 Mutation in a Croatian boy with Brachytelephalangy and a Thin Corpus Callosum. Human Genome Variation, 5., 1-4. doi: 10.1038/hgv.2018.5
Sakaguchi, Tomohiro, et al. "A Novel PGAP3 Mutation in a Croatian boy with Brachytelephalangy and a Thin Corpus Callosum." Human Genome Variation, vol. 5, 2018, pp. 1-4. https://doi.org/10.1038/hgv.2018.5
Sakaguchi, Tomohiro, Tamara Žigman, Danijela Petković Ramadža, Lana Omerza, Silvija Pušeljić, Zrinka Ereš Hrvaćanin, Noriko Miyake, Naomichi Matsumoto and Ivo Barić. "A Novel PGAP3 Mutation in a Croatian boy with Brachytelephalangy and a Thin Corpus Callosum." Human Genome Variation 5 (2018): 1-4. https://doi.org/10.1038/hgv.2018.5
Sakaguchi, T., et al. (2018) 'A Novel PGAP3 Mutation in a Croatian boy with Brachytelephalangy and a Thin Corpus Callosum', Human Genome Variation, 5, pp. 1-4. doi: 10.1038/hgv.2018.5
Sakaguchi T, Žigman T, Petković Ramadža D, Omerza L, Pušeljić S, Ereš Hrvaćanin Z, and sur.. A Novel PGAP3 Mutation in a Croatian boy with Brachytelephalangy and a Thin Corpus Callosum. Human Genome Variation [Internet]. 2018 [cited 2024 November 18];5:1-4. doi: 10.1038/hgv.2018.5
T. Sakaguchi, et al., "A Novel PGAP3 Mutation in a Croatian boy with Brachytelephalangy and a Thin Corpus Callosum", Human Genome Variation, vol. 5, pp. 1-4, 2018. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:239:345932. [Accessed: 18 November 2024]
