APA استشهاد

A., S., C., S., M., P., K., S., & V., S. (2017). Whole-exome sequencing reveals a novel COL2A1 mutation in a patient with spondyloepiphyseal dysplasia congenita.

استشهاد بنمط شيكاغو

A., Sangsin, Srichomthong C., Pongpanich M., Suphapeetiporn K., و Shotelersuk V. Whole-exome Sequencing Reveals a Novel COL2A1 Mutation in a Patient With Spondyloepiphyseal Dysplasia Congenita. 2017.

MLA استشهاد

A., Sangsin, et al. Whole-exome Sequencing Reveals a Novel COL2A1 Mutation in a Patient With Spondyloepiphyseal Dysplasia Congenita. 2017.

تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.