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	101.	Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. Online. [electronic resource] by Arrendondo-Vega, F X Santisteban, I Notarangelo, L D El Dahr, J Buckley, R Roifman, C Conley, M E Hershfield, M S Producer: 19990405 In: Human mutation vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Expression of the gene defect in X-linked agammaglobulinemia. [electronic resource] by Conley, M E Brown, P Pickard, A R Buckley, R H Miller, D S Raskind, W H Singer, J W Fialkow, P J Producer: 19860917 In: The New England journal of medicine vol. 315 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	103.	Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22. [electronic resource] by Parolini, O Hejtmancik, J F Allen, R C Belmont, J W Lassiter, G L Henry, M J Barker, D F Conley, M E Producer: 19930414 In: Genomics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	104.	Cure of X-linked lymphoproliferative disease (XLP) with allogeneic hematopoietic stem cell transplantation (HSCT): report from the XLP registry. [electronic resource] by Gross, T G Filipovich, A H Conley, M E Pracher, E Schmiegelow, K Verdirame, J D Vowels, M Williams, L L Seemayer, T A Producer: 19961106 In: Bone marrow transplantation vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	105.	Hyper IgM syndrome associated with defective CD40-mediated B cell activation. [electronic resource] by Conley, M E Larché, M Bonagura, V R Lawton, A R Buckley, R H Fu, S M Coustan-Smith, E Herrod, H G Campana, D Producer: 19941110 In: The Journal of clinical investigation vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	106.	Mutations in the mu heavy-chain gene in patients with agammaglobulinemia. [electronic resource] by Yel, L Minegishi, Y Coustan-Smith, E Buckley, R H Trübel, H Pachman, L M Kitchingman, G R Campana, D Rohrer, J Conley, M E Producer: 19961121 In: The New England journal of medicine vol. 335 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	Membranous glomerulopathy in an adult patient with X-linked agammaglobulinemia receiving intravenous gammaglobulin. [electronic resource] by Endo, L M Giannobile, J V Dobbs, A K Foote, J B Szymanska, E Warnock, D G Cook, W J Conley, M E Schroeder, H W Producer: 20111011 In: Journal of investigational allergology & clinical immunology vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	108.	A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome. [electronic resource] by Lin, Q Rohrer, J Allen, R C Larché, M Greene, J M Shigeoka, A O Gatti, R A Derauf, D C Belmont, J W Conley, M E Producer: 19960216 In: The Journal of clinical investigation vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	Relationship of the genes for Chediak-Higashi syndrome (beige) and the T-cell receptor gamma chain in mouse and man. [electronic resource] by Holcombe, R F Strauss, W Owen, F L Boxer, L A Warren, R W Conley, M E Ferrara, J Leavitt, R Y Fauci, A S Taylor, B A Producer: 19880526 In: Genomics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome. [electronic resource] by Allen, R C Armitage, R J Conley, M E Rosenblatt, H Jenkins, N A Copeland, N G Bedell, M A Edelhoff, S Disteche, C M Simoneaux, D K Producer: 19930322 In: Science (New York, N.Y.) vol. 259 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome. [electronic resource] by Minegishi, Y Lavoie, A Cunningham-Rundles, C Bédard, P M Hébert, J Côté, L Dan, K Sedlak, D Buckley, R H Fischer, A Durandy, A Conley, M E Producer: 20010111 In: Clinical immunology (Orlando, Fla.) vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	112.	Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency. [electronic resource] by Puck, J M Pepper, A E Henthorn, P S Candotti, F Isakov, J Whitwam, T Conley, M E Fischer, R E Rosenblatt, H M Small, T N Buckley, R H Producer: 19970402 In: Blood vol. 89 Availability: No items available. Save to lists Add to cart (remove)
	113.	Molecular evidence of ocular Epstein-Barr virus infection. [electronic resource] by Slobod, K S Sandlund, J T Spiegel, P H Haik, B Hurwitz, J L Conley, M E Bowman, L C Benaim, E Jenkins, J J Stocks, R M Gan, Y Sixbey, J W Producer: 20001103 In: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	114.	X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling. [electronic resource] by Döffinger, R Smahi, A Bessia, C Geissmann, F Feinberg, J Durandy, A Bodemer, C Kenwrick, S Dupuis-Girod, S Blanche, S Wood, P Rabia, S H Headon, D J Overbeek, P A Le Deist, F Holland, S M Belani, K Kumararatne, D S Fischer, A Shapiro, R Conley, M E Reimund, E Kalhoff, H Abinun, M Munnich, A Israël, A Courtois, G Casanova, J L Producer: 20010412 In: Nature genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	115.	V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations. [electronic resource] by Villa, A Sobacchi, C Notarangelo, L D Bozzi, F Abinun, M Abrahamsen, T G Arkwright, P D Baniyash, M Brooks, E G Conley, M E Cortes, P Duse, M Fasth, A Filipovich, A M Infante, A J Jones, A Mazzolari, E Muller, S M Pasic, S Rechavi, G Sacco, M G Santagata, S Schroeder, M L Seger, R Strina, D Ugazio, A Väliaho, J Vihinen, M Vogler, L B Ochs, H Vezzoni, P Friedrich, W Schwarz, K Producer: 20010215 In: Blood vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	Loss of B Cells in Patients with Heterozygous Mutations in IKAROS. [electronic resource] by Kuehn, H S Boisson, B Cunningham-Rundles, C Reichenbach, J Stray-Pedersen, A Gelfand, E W Maffucci, P Pierce, K R Abbott, J K Voelkerding, K V South, S T Augustine, N H Bush, J S Dolen, W K Wray, B B Itan, Y Cobat, A Sorte, H S Ganesan, S Prader, S Martins, T B Lawrence, M G Orange, J S Calvo, K R Niemela, J E Casanova, J-L Fleisher, T A Hill, H R Kumánovics, A Conley, M E Rosenzweig, S D Producer: 20160322 In: The New England journal of medicine vol. 374 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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