Shariati, G., Saberi, A., Hamid, M., Galehdari, H., Sedaghat, A., & Abdorasuli, N. (2018). Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH. Clin Case Rep.

Shariati, Gholamreza, Alihossein Saberi, Mohammad Hamid, Hamid Galehdari, Alireza Sedaghat, and Nehzat Abdorasuli. "Prenatal Diagnosis of a Rare De Novo 1q22‐q25.1 Chromosomal Deletion Syndrome Using Oligo Array CGH." Clin Case Rep 2018.

Shariati, Gholamreza, et al. "Prenatal Diagnosis of a Rare De Novo 1q22‐q25.1 Chromosomal Deletion Syndrome Using Oligo Array CGH." Clin Case Rep 2018.