T Cell Transcriptome in Chromosome 22q11.2 Deletion Syndrome by Raje, Nikita R., Noel-MacDonnell, Janelle R., Shortt, Katherine A., Gigliotti, Nicole M., Chan, Marcia A., Heruth, Daniel P.

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HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory disease by Cook, Sarah A, Comrie, William A, Poli, M Cecilia, Similuk, Morgan, Oler, Andrew J, Faruqi, Aiman J, Kuhns, Douglas B, Yang, Sheng, Vargas-Hernández, Alexander, Carisey, Alexandre F, Fournier, Benjamin, Anderson, D Eric, Price, Susan, Smelkinson, Margery, Abou Chahla, Wadih, Forbes, Lisa R, Mace, Emily M, Cao, Tram N, Coban-Akdemir, Zeynep H, Jhangiani, Shalini N, Muzny, Donna M, Gibbs, Richard A, Lupski, James R, Orange, Jordan S, Cuvelier, Geoffrey D E, Al Hassani, Moza, Al Kaabi, Nawal, Al Yafei, Zain, Jyonouchi, Soma, Raje, Nikita, Caldwell, Jason W, Huang, Yanping, Burkhardt, Janis K, Latour, Sylvain, Chen, Baoyu, ElGhazali, Gehad, Rao, V Koneti, Chinn, Ivan K, Lenardo, Michael J

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Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the Am... by Chinn, Ivan K., Chan, Alice Y., Chen, Karin, Chou, Janet, Dorsey, Morna J., Hajjar, Joud, Jongco, Artemio M., Keller, Michael D., Kobrynski, Lisa J., Kumanovics, Attila, Lawrence, Monica G., Leiding, Jennifer W., Lugar, Patricia L., Orange, Jordan S., Patel, Kiran, Platt, Craig D., Puck, Jennifer M., Raje, Nikita, Romberg, Neil, Slack, Maria A., Sullivan, Kathleen E., Tarrant, Teresa K., Torgerson, Troy R., Walter, Jolan E.

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