Cite
MLA Citation
Andrea Martin‐Nalda et al.. “Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain).” Molecular genetics & genomic medicine, vol. 7, no. 12, 2019, p. n/a. http://access.bl.uk/ark:/81055/vdc_100098072317.0x000005