Statements in which the resource exists.
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pubmed-article:10588839pubmed:abstractTextWe report on a new patient with deletion of 22q11 associated with hemophagocytic lymphohistiocytosis and a fatal outcome. She had minor facial anomalies and cardiac malformation corresponding to those described in del (22q11) syndrome, normal T and B cell function and NK activity; bone marrow aspiration showed active erythrophagocytosis. Our case in addition to two other children reported previously suggest that such a rare association between lymphocyte-macrophage activation and deletion of 22q11 may be more frequent than previously recognized.lld:pubmed
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pubmed-article:10588839pubmed:authorpubmed-author:ClementsDDlld:pubmed
pubmed-article:10588839pubmed:copyrightInfoCopyright 1999 Wiley-Liss, Inc.lld:pubmed
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pubmed-article:10588839pubmed:pagination329-30lld:pubmed
pubmed-article:10588839pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:10588839pubmed:year1999lld:pubmed
pubmed-article:10588839pubmed:articleTitleHemophagocytic lymphohistiocytosis in a patient with deletion of 22q11.2.lld:pubmed
pubmed-article:10588839pubmed:affiliationClinica Pediatrica, IRCCS Policlinico S. Matteo, Pavia, Italy.lld:pubmed
pubmed-article:10588839pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10588839pubmed:publicationTypeCase Reportslld:pubmed
pubmed-article:10588839pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed