APA (7th ed.) Citation

Somprakash Dhangar, Purvi Panchal, Jagdeeshwar Ghatanatti, Jitendra Suralkar, Anjali Shah, & Babu Rao Vundinti. (2022). Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations. BMC.

Chicago Style (17th ed.) Citation

Somprakash Dhangar, Purvi Panchal, Jagdeeshwar Ghatanatti, Jitendra Suralkar, Anjali Shah, and Babu Rao Vundinti. Novel Deletion of Exon 3 in TYR gene Causing Oculocutaneous Albinism 1B in an Indian Family Along with Intellectual Disability Associated with Chromosomal Copy Number Variations. BMC, 2022.

MLA (9th ed.) Citation

Somprakash Dhangar, et al. Novel Deletion of Exon 3 in TYR gene Causing Oculocutaneous Albinism 1B in an Indian Family Along with Intellectual Disability Associated with Chromosomal Copy Number Variations. BMC, 2022.