Expanding the nude SCID/CID phenotype associated with FOXN1 homozygous, compound heterozygous, or heterozygous mutations מאת Giardino, G, Sharapova, SO, Ciznar, P, Dhalla, F, Maragliano, L, Radha Rama Devi, A, Islamoglu, C, Ikinciogullari, A, Haskologlu, S, Dogu, F, Hanna-Wakim, R, Dbaibo, G, Chou, J, Cirillo, E, Borzacchiello, C, Kreins, AY, Worth, A, Rota, IA, Marques, JG, Sayitoglu, M, Firtina, S, Mahdi, M, Geha, R, Neven, B, Sousa, AE, Benfenati, F, Hollander, GA, Davies, EG, Pignata, C