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[A 32:1 chance for the linkage of this rare IgH haplotype with the hyper-IgG1(A1) syndrome in the family argues for a dominant regulator located at the human IgH locus having a selective influence on the production of IgG1 and IgA1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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