Cite
MLA Citation
Gholamreza Shariati et al.. “Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH.” Clinical case reports, vol. 6, no. 8, 2018, pp. 1464–1469. http://access.bl.uk/ark:/81055/vdc_100068501557.0x000009