Items where authors include "Lawless, D."

Article

Lawless, D., Geier, C.B., Farmer, J.R. et al. (43 more authors) (2018) Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency. Journal of Allergy and Clinical Immunology, 141 (6). pp. 2303-2306. ISSN 0091-6749

Proceedings Paper

Poulter, J., Nadat, F., O'Callaghan, E. et al. (13 more authors) (2024) P13.018.D Biallelic mutation of CWF19L2, encoding a core spliceosome subunit, causes a combined neurodevelopmental and immunodeficiency disorder. In: European Journal of Human Genetics. 57th European Society of Human Genetics (ESHG) Conference, 01-04 Jun 2024, Berlin, Germany. .