Engelhardt, K. R.Gertz, E. M.Keleş, S.Schaeffer, Alejandro A.Ceja, R.Sassi, A.Massaad, M. J.Mellouli, F.Benmustapha, I.Khemiri, M.Etzioni, A.Freeman, A. F.Thiel, J.Schulze, I.Al-Herz, W.Metin, A.Sanal, O.Yeganeh, M.Niehues, T.Siepermann, K.Ünal, E.Patıroğlu, T.Dasouki, M.Yılmaz, MustafaGenel, F.Aytekin, C.Kütükçüler, N.Somer, AyperKılıç, M.Reisli, I.Camcıoğlu, Y.Gennery, A. R.Cant, A. J.Jones, A.Gaspar, H. B.Arkwright, P. D.Pietrogrande, M. C.Baz, Z.Al-Tamemi, SalemLougaris, V.Lefranc, G.Megarbane, AndreBoutros, J.Galal, N.Bejaoui, MohamedBarbouche, R.Geha, R. S.Chatila, T. A.Grimbacher, B.2022-10-052022-10-052012-09Engelhardt, K. R. vd. (2012). "Dock8 deficiency and a diagnostic score to differentiate it from other Hyper-IGE syndromes". Journal of Clinical Immunology, 32, Supplement 1, 332-333.0271-9142http://hdl.handle.net/11452/28966Bu çalışma, 3-6 Ekim 2012'de Floransa[İtalya]'da düzenlenen 15. Biennial Meeting European-Society-for-Immunodeficiency (ESID)'de bildiri olarak sunulmuştur.eninfo:eu-repo/semantics/closedAccessImmunologyArticle00030872890067733233332Supplement 1Immunology