Severe combined immunodeficiencies, primary T-cell defects and DiGeorge syndrome in humans: Characterization by monoclonal antibodies and natural killer cell activity-Reference-Cited by-同舟云学术

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Severe combined immunodeficiencies, primary T-cell defects and DiGeorge syndrome in humans: Characterization by monoclonal antibodies and natural killer cell activity

Published:1983-09 Issue:3 Volume:28 Page:361-370
ISSN:0090-1229
Container-title:Clinical Immunology and Immunopathology
language:en
Short-container-title:Clinical Immunology and Immunopathology

Author:

Sirianni M.C.,Businco L.,Seminara R.,Aiuti F.

Publisher

Elsevier BV

Subject

Immunology,Pathology and Forensic Medicine,Immunology and Allergy

Reference21 articles.

1. Primary Immunodeficiencies;Reinherz,1981

2. A population of sheep rosetting cells lacking T- and monocytic-specific antigens, as detected by monoclonal antibodies

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