More than just SCID-The phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2NIEHUES, Tim; PEREZ-BECKER, Ruy; SCHUETZ, Catharina et al.Clinical immunology (Orlando, Fla. Print). 2010, Vol 135, Num 2, pp 183-192, issn 1521-6616, 10 p.Article

Successful unrelated bone marrow transplantation in a child with chronic granulomatous disease complicated by pulmonary and cerebral granuloma formationSCHUETZ, Catharina; HOENIG, Manfred; SCHUIZ, Ansgar et al.European journal of pediatrics. 2007, Vol 166, Num 8, pp 785-788, issn 0340-6199, 4 p.Article

Lesson from hypomorphic recombination-activating gene (RAG) mutations: Why asymptomatic siblings should also be testedSCHUETZ, Catharina; PANNICKE, Ulrich; FRIEDRICH, Wilhelm et al.Journal of allergy and clinical immunology. 2014, Vol 133, Num 4, pp 1211-1215, issn 0091-6749, 5 p.Article

Mutations in ZBTB24 Are Associated with Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome Type 2DE GREEF, Jessica C; JUN WANG; GENNERY, Andrew R et al.American journal of human genetics. 2011, Vol 88, Num 6, pp 796-804, issn 0002-9297, 9 p.Article

An Immunodeficiency Disease with RAG Mutations and GranulomasSCHUETZ, Catharina; HUCK, Kirsten; KNÜCHEL, Ruth et al.The New England journal of medicine. 2008, Vol 358, Num 19, pp 2030-2038, issn 0028-4793, 9 p.Article