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Journal of Immunology (Baltimore, Md. : 1950)|December 15, 1996
Genomic structure and mapping of human FADD, an intracellular mediator of lymphocyte apoptosisP K Kim, A S Dutra, S C Chandrasekharappa, et al.
American Journal of Human Genetics|May 1, 1989
X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysisJ M Puck, R L Nussbaum, D L Smead, et al.
The Journal of Pediatrics|September 1, 1991
Molecular analysis of X-linked agammaglobulinemia with growth hormone deficiencyM E Conley, A W Burks, H G Herrod, et al.
American Journal of Human Genetics|September 1, 1995
Two mutational hotspots in the interleukin-2 receptor gamma chain gene causing human X-linked severe combined immunodeficiencyA E Pepper, R H Buckley, T N Small, et al.
The Journal of Infectious Diseases|December 1, 1980
Protection of infants from infection with influenza A virus by transplacentally acquired antibodyJ M Puck, W P Glezen, A L Frank, et al.
Clinical Immunology and Immunopathology|June 1, 1990
X chromosome inactivation patterns in obligate carriers of X-linked lymphoproliferative syndromeM E Conley, J L Sullivan, J A Neidich, et al.
Molecular Immunology|January 1, 1991
Modification in framework region I results in a decreased affinity of chimeric anti-TAG72 antibodyJ H Xiang, J Roder, Z G Pan, et al.
Therapeutic Drug Monitoring|June 1, 1987
Corticosteroids-salicylate interaction in a case of juvenile rheumatoid arthritisG Koren, C Roifman, E Gelfand, et al.
Annals of Internal Medicine|April 3, 1999
An inherited disorder of lymphocyte apoptosis: the autoimmune lymphoproliferative syndromeS E Straus, M Sneller, M J Lenardo, et al.
Israel Journal of Medical Sciences|June 1, 1984
Sinus node dysfunction in a healthy pediatric populationC Roifman, L Dembo, E Grenadier, et al.
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