Cite

    Keiko Shimojima et al.. “A 10q21.3q22.2 microdeletion identified in a patient with severe developmental delay and multiple congenital anomalies including congenital heart defects.” Congenital anomalies, vol. 58, 2018, pp. 36–38. http://access.bl.uk/ark:/81055/vdc_100055655615.0x000036