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	81.	Direct quantitation of IgG subclasses 1, 2, and 3 bound to red cells by Rh1 (D) antibodies. [electronic resource] by Shaw, D R Conley, M E Knox, F J Khazaeli, M B LoBuglio, A F Producer: 19880512 In: Transfusion vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	Prenatal test for X-linked severe combined immunodeficiency by analysis of maternal X-chromosome inactivation and linkage analysis. [electronic resource] by Puck, J M Krauss, C M Puck, S M Buckley, R H Conley, M E Producer: 19900427 In: The New England journal of medicine vol. 322 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	A chromosomal breakage syndrome with profound immunodeficiency. [electronic resource] by Conley, M E Spinner, N B Emanuel, B S Nowell, P C Nichols, W W Producer: 19860606 In: Blood vol. 67 Availability: No items available. Save to lists Add to cart (remove)
	84.	Atypical presentation of Wiskott-Aldrich syndrome: diagnosis in two unrelated males based on studies of maternal T cell X chromosome inactivation. [electronic resource] by Puck, J M Siminovitch, K A Poncz, M Greenberg, C R Rottem, M Conley, M E Producer: 19900718 In: Blood vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	85.	Atypical Wiskott-Aldrich syndrome in a girl. [electronic resource] by Conley, M E Wang, W C Parolini, O Shapiro, D N Campana, D Siminovitch, K A Producer: 19921006 In: Blood vol. 80 Availability: No items available. Save to lists Add to cart (remove)
	86.	Mutations in the human lambda5/14.1 gene result in B cell deficiency and agammaglobulinemia. [electronic resource] by Minegishi, Y Coustan-Smith, E Wang, Y H Cooper, M D Campana, D Conley, M E Producer: 19980127 In: The Journal of experimental medicine vol. 187 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia. [electronic resource] by Rohrer, J Parolini, O Belmont, J W Conley, M E Parolino O [corrected to Parolini, O ] Producer: 19941108 In: Immunogenetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	A newly recognized, likely autosomal recessive syndrome comprising agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis, and other features. [electronic resource] by Crow, Yanick Joseph Goodship, J A Wright, C Coady, A M Conley, M E Gennery, A R Producer: 20060727 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	89.	The transcription factor Bright associates with Bruton's tyrosine kinase, the defective protein in immunodeficiency disease. [electronic resource] by Webb, C F Yamashita, Y Ayers, N Evetts, S Paulin, Y Conley, M E Smith, E A Producer: 20010125 In: Journal of immunology (Baltimore, Md. : 1950) vol. 165 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	Variations in the human phospholipase Cgamma2 gene in patients with B-cell defects of unknown etiology. [electronic resource] by Wang, D Boylin, E C Minegishi, Y Wen, R Smith, C I Ihle, J N Conley, M E Producer: 20011226 In: Immunogenetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	A minimally hypomorphic mutation in Btk resulting in reduced B cell numbers but no clinical disease. [electronic resource] by Conley, M E Farmer, D M Dobbs, A K Howard, V Aiba, Y Shurtleff, S A Kurosaki, T Producer: 20080512 In: Clinical and experimental immunology vol. 152 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	Correction of Duncan's syndrome by allogeneic bone marrow transplantation. [electronic resource] by Williams, L L Rooney, C M Conley, M E Brenner, M K Krance, R A Heslop, H E Producer: 19930923 In: Lancet (London, England) vol. 342 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	Monoclonal antibodies against isotypic and isoallotypic determinants of human IgA1 and IgA2: fine specificities and binding properties. [electronic resource] by Delacroix, D L Van Snick, J Vaerman, J P Conley, M E Mascart-Lemone, F Bernier, G M Producer: 19860820 In: Molecular immunology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	94.	Frequent mutations in SH2D1A (XLP) in males presenting with high-grade mature B-cell neoplasms. [electronic resource] by Sandlund, J T Shurtleff, S A Onciu, M Horwitz, E Leung, W Howard, V Rencher, R Conley, M E Producer: 20130923 In: Pediatric blood & cancer vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	95.	A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafness. [electronic resource] by Richter, D Conley, M E Rohrer, J Myers, L A Zahradka, K Kelecić, J Sertić, J Stavljenić-Rukavina, A Producer: 20010913 In: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	96.	CD38 signal transduction in human B cell precursors. Rapid induction of tyrosine phosphorylation, activation of syk tyrosine kinase, and phosphorylation of phospholipase C-gamma and phosphatidylinositol 3-kinase. [electronic resource] by Silvennoinen, O Nishigaki, H Kitanaka, A Kumagai, M Ito, C Malavasi, F Lin, Q Conley, M E Campana, D Producer: 19960423 In: Journal of immunology (Baltimore, Md. : 1950) vol. 156 Availability: No items available. Save to lists Add to cart (remove)
	97.	An essential role for BLNK in human B cell development. [electronic resource] by Minegishi, Y Rohrer, J Coustan-Smith, E Lederman, H M Pappu, R Campana, D Chan, A C Conley, M E Producer: 19991216 In: Science (New York, N.Y.) vol. 286 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	98.	Mutations of the human BTK gene coding for bruton tyrosine kinase in X-linked agammaglobulinemia. [electronic resource] by Vihinen, M Kwan, S P Lester, T Ochs, H D Resnick, I Väliaho, J Conley, M E Smith, C I Producer: 19990610 In: Human mutation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	99.	Brief report: a point mutation in the SH2 domain of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia. [electronic resource] by Saffran, D C Parolini, O Fitch-Hilgenberg, M E Rawlings, D J Afar, D E Witte, O N Conley, M E Producer: 19940526 In: The New England journal of medicine vol. 330 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	100.	X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings. [electronic resource] by Conley, M E Buckley, R H Hong, R Guerra-Hanson, C Roifman, C M Brochstein, J A Pahwa, S Puck, J M Producer: 19900606 In: The Journal of clinical investigation vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 116 results.