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Citation: Cl. Bennett et al., A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA -> AAUGAA) leads to the IPEX syndrome, IMMUNOGENET, 53(6), 2001, pp. 435-439

Authors: Harris, ES Shigeoka, AO Li, WH Adams, RH Prescott, SM McIntyre, TM Zimmerman, GA Lorant, DE

Citation: Es. Harris et al., A novel syndrome of variant leukocyte adhesion deficiency involving defects in adhesion mediated by beta(1) and beta(2) integrins, BLOOD, 97(3), 2001, pp. 767-776

Authors: Adderson, EE Viskochil, DH Carey, JC Shigeoka, AO Christenson, JC Bohnsack, JF Hill, HR

Citation: Ee. Adderson et al., Growth failure, intracranial calcifications, acquired pancytopenia, and unusual humoral immunodeficiency: A genetic syndrome?, AM J MED G, 95(1), 2000, pp. 17-20

Authors: Bennett, CL Yoshioka, R Kiyosawa, H Barker, DF Fain, PR Shigeoka, AO Chance, PF

Citation: Cl. Bennett et al., X-linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3, AM J HU GEN, 66(2), 2000, pp. 461-468