APA način citiranja

Giri, D., Rigden, D., Didi, M., Peak, M., McNamara, P., & Senniappan, S. (2017). Novel compound heterozygous ASXL3 mutation causing Bainbridge-ropers like syndrome and primary IGF1 deficiency. Int J Pediatr Endocrinol.

Čikaški stil citiranja

Giri, Dinesh, Daniel Rigden, Mohammed Didi, Matthew Peak, Paul McNamara, i Senthil Senniappan. "Novel Compound Heterozygous ASXL3 Mutation Causing Bainbridge-ropers Like Syndrome and Primary IGF1 Deficiency." Int J Pediatr Endocrinol 2017.

MLA način citiranja

Giri, Dinesh, et al. "Novel Compound Heterozygous ASXL3 Mutation Causing Bainbridge-ropers Like Syndrome and Primary IGF1 Deficiency." Int J Pediatr Endocrinol 2017.