APA Style

Khatun, D, M. (2020). Identification of Mutation in Exon2 of the NKX2.5 Gene in Bangladeshi Pediatric Patients with Congenital Hypothyroidism . BSMMU: Dr. Marjia Khatun.

MLA Style

Khatun, Dr., Marjia. "Identification of Mutation in Exon2 of the NKX2.5 Gene in Bangladeshi Pediatric Patients with Congenital Hypothyroidism". BSMMU: Dr. Marjia Khatun, 2020. Thesis.