Alison M. Jones

Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2Rγ chain gene by single-strand conformation polymorphism analysis

R. Levinsky, P. Clark, R. Hendriks, 1995, Human Genetics.

immunodeficiencies haematopoietic stem cell transplantation for severe congenital Cognitive and behavioural abnormalities in children following

T. Cole, P. Veys, A. Thrasher, 2013 .

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.

A. Schäffer, V. Lougaris, R. Geha, 2015, The Journal of allergy and clinical immunology.

Improved survival after unrelated donor bone marrow transplantation in children with primary immunodeficiency using a reduced-intensity conditioning regimen.

P. Veys, P. Amrolia, C. Cale, 2005, Blood.

Clinical picture and treatment of 2212 patients with common variable immunodeficiency.

É. Oksenhendler, P. Soler-Palacín, A. Šedivá, 2014, The Journal of allergy and clinical immunology.

Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single center.

G. Giardino, A. Worth, Winnie Ip, 2019, Blood.

The many faces of Artemis-deficient combined immunodeficiency - Two patients with DCLRE1C mutations and a systematic literature review of genotype-phenotype correlation.

P. Jeggo, P. Veys, P. Amrolia, 2013, Clinical immunology.

Immunodeficiency and disseminated mycobacterial infection associated with homozygous nonsense mutation of IKKβ☆

S. Nejentsev, V. Plagnol, S. Burns, 2014, The Journal of allergy and clinical immunology.

Severe combined immunodeficiency with abnormalities in expression of the common leucocyte antigen, CD45

P. Veys, N. Klein, C. Cale, 1997, Archives of disease in childhood.