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Journal of Experimental Medicine, Vol 174, 1039-1048, Copyright © 1991 by Rockefeller University Press
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K Schwarz, TE Hansen-Hagge, C Knobloch, W Friedrich, E Kleihauer and CR Bartram
Section of Molecular Biology, University of Ulm, Germany.
Human severe combined immunodeficiency (SCID) patients were analyzed by a polymerase chain reaction assay for their recombination capability at the DHQ52-JH region of the immunoglobulin heavy chain locus. Five patients with B cells (B+ SCID) exhibited a recombination pattern also observed in healthy persons. In contrast, six patients lacking B cells (B- SCID) showed a grossly altered rearrangement pattern characterized by the (partial) absence of regular DHQ52-JH recombinations and the presence of abnormal rearrangements. These events were caused by deletions surpassing the boundaries of immunoglobulin coding elements and thus resemble the pattern of deletional recombinations previously described in SCID mice.
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