Mechanisms of Tolerance to Parental Parathyroid Tissue when Combined with Human Allogeneic Thymus Transplantation von Chinn, I.K, Olson, J.A, Skinner, M.A, McCarthy, E.A, Gupton, S.E, Bonilla, F.A, Roberts, R.L, Kanariou, M.G, Devlin, B.H, Markert, M.L

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Combined Thymus and Parathyroid Allotransplantation in Complete DiGeorge Anomaly von Chinn, I.K, Olson, J.A, Skinner, M.A, McCarthy, E.A, Gupton, S.E, Bonilla, F.A, Roberts, R.L, Kanariou, M.G, Devlin, B.H, Markert, M.L

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Tolerance To Allogeneic Thymus Transplantation In Complete DiGeorge Syndrome von Chinn, I.K, Devlin, B.H, Alexieff, M.J, Li, J, Gupton, S.E, McCarthy, E.A, Markert, M.L

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Factors Affecting Success of Thymus Transplantation for Complete DiGeorge Anomaly von Markert, M. L., Devlin, B. H., Chinn, I. K., McCarthy, E. A., Li, Y. J.

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Parathyroid Gland Transplantation without Posttransplantation Immunosuppression von Chinn, I.K., Devlin, B.H., Alexieff, M.A., Li, J., McCarthy, E., Skinner, M.A., Olson, J.A., Markert, M.L.

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Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency von Saettini, F., Poli, C., Vengoechea, J., Bonanomi, S., Orellana, J.C., Fazio, G., Rodriguez, F.H., Noguera, L.P., Booth, C., Jarur-Chamy, V., Shams, M., Iascone, M., Vukic, M., Gasperini, S., Quadri, M., Seijas, A.B., Rivers, E., Mauri, M., Badolato, R., Cazzaniga, G., Bugarin, C., Gaipa, G., Kroes, W.G.M., Moratto, D., Ostaijen-ten Dam, M.M. van, Baas, F., Maarel, S. van der, Piazza, R., Coban-Akdemir, Z.H., Lupski, J.R., Yuan, B., Chinn, I.K., Daxinger, L., Biondi, A.

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Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome von Weerts, M.J.A., Lanko, K., Guzman-Vega, F.J., Jackson, A., Ramakrishnan, R., Cardona-Londono, K.J., Pena-Guerra, K.A., Bever, Y. van, Paassen, B.W. van, Kievit, A., Slegtenhorst, M. van, Allen, N.M., Kehoe, C.M., Robinson, H.K., Pang, L., Banu, S.H., Zaman, M., Efthymiou, S., Houlden, H., Jarvela, I., Lauronen, L., Maatta, T., Schrauwen, I., Leal, S.M., Ruivenkamp, C.A.L., Barge-Schaapveld, D.Q.C.M., Peeters-Scholte, C.M.P.C.D., Galehdari, H., Mazaheri, N., Sisodiya, S.M., Harrison, V., Sun, A., Thies, J., Pedroza, L.A., Lara-Taranchenko, Y., Chinn, I.K., Lupski, J.R., Garza-Flores, A., McGlothlin, J., Yang, L., Huang, S.P., Wang, X.D., Jewett, T., Rosso, G., Lin, X., Mohammed, S., Merritt, J.L., Mirzaa, G.M., Timms, A.E., Scheck, J., Elting, M.W., Polstra, A.M., Schenck, L., Ruzhnikov, M.R.Z., Vetro, A., Montomoli, M., Guerrini, R., Koboldt, D.C., Mosher, T.M., Pastore, M.T., McBride, K.L., Peng, J., Pan, Z., Willemsen, M., Koning, S., Turnpenny, P.D., Vries, B.B.A. de, Gilissen, C., Pfundt, R., Lees, M., Braddock, S.R., Klemp, K.C., Vansenne, F., Gijn, M.E. van, Quindipan, C., Deardorff, M.A., Hamm, J.A., Putnam, A.M., Baud, R., Walsh, L., Lynch, S.A., Baptista, J., Person, R.E., Monaghan, K.G., Crunk, A., Keller-Ramey, J., Reich, A., Elloumi, H.Z., Alders, M., Kerkhof, J., McConkey, H., Haghshenas, S., Maroofian, R., Sadikovic, B., Banka, S., Arold, S.T., Barakat, T.S.

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Bi-allelic variants in TONSL cause SPONASTRIME dysplasia and a spectrum of skeletal dysplasia phenotypes von Burrage, L.C, Reynolds, J.J, Baratang, N.V, Phillips, J.B, Wegner, J, McFarquhar, A, Higgs, M.R, Christiansen, A.E, Lanza, D.G, Seavitt, J.R, Jain, M, Li, X, Parry, D.A, Raman, V, Chitayat, D, Chinn, I.K, Bertuch, A.A, Karaviti, L, Schlesinger, A.E, Earl, D, Bamshad, M, Savarirayan, R, Doddapaneni, H, Muzny, D, Jhangiani, S.N, Eng, C.M, Gibbs, R.A, Bi, W, Emrick, L, Rosenfeld, J.A, Postlethwait, J, Westerfield, M, Dickinson, M.E, Beaudet, A.L, Ranza, E, Huber, C, Cormier-Daire, V, Shen, W, Mao, R, Heaney, J.D, Orange, J.S, University of Washington Center for Mendelian Genomics, Undiagnosed Diseases Network, Bertola, D, Yamamoto, G.L, Baratela, W.A.R, Butler, M.G, Ali, A, Adeli, M, Cohn, D.H, Krakow, D, Jackson, A.P, Lees, M, Offiah, A.C, Carlston, C.M, Carey, J.C, Stewart, G.S, Bacino, C.A, Campeau, P.M, Lee, B

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