| Literature DB >> 3263154 |
E R Fearon1, D B Kohn, J A Winkelstein, B Vogelstein, R M Blaese.
Abstract
The Wiskott-Aldrich syndrome (WAS) is an X-linked recessive disease characterized by immunodeficiency and severe thrombocytopenia in affected males, but no demonstrable clinical abnormalities in carrier females. Through analysis of the methylation patterns of X-linked genes that display restriction fragment length polymorphisms (RFLPs), we studied the pattern of X-chromosome inactivation in various cell populations from female relatives of patients with WAS. The peripheral blood T cells, granulocytes, and B cells of eight obligate WAS carriers were found to display specific patterns of X-chromosome inactivation clearly different from these of normal controls. Thus, carriers of WAS could be accurately identified using this analysis.Entities:
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Year: 1988 PMID: 3263154
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113