X-linked severe combined immunodeficiency
- 30 November 1991
- journal article
- review article
- Published by Elsevier in Clinical Immunology and Immunopathology
- Vol. 61 (2) , S94-S99
- https://doi.org/10.1016/s0090-1229(05)80043-1
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
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- Prenatal Test for X-Linked Severe Combined Immunodeficiency by Analysis of Maternal X-Chromosome Inactivation and Linkage AnalysisNew England Journal of Medicine, 1990
- Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency.Proceedings of the National Academy of Sciences, 1988
- USE OF X CHROMOSOME INACTIVATION ANALYSIS TO ESTABLISH CARRIER STATUS FOR X-LINKED SEVERE COMBINED IMMUNODEFICIENCYThe Lancet, 1988
- Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.Proceedings of the National Academy of Sciences, 1987
- Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation.Journal of Clinical Investigation, 1987
- XX T cells and XY B cells in two patients with severe combined immune deficiencyClinical Immunology and Immunopathology, 1984
- Identification by HLA Typing of Intrauterine-Derived Maternal T Cells in Four Patients with Severe Combined ImmunodeficiencyNew England Journal of Medicine, 1982
- Selective defect of precursor T cells associated with apparently normal B lymphocytes in severe combined immunodeficiency diseaseThe Journal of Pediatrics, 1978
- THE THYMUS AND OTHER LYMPHOID TISSUES IN CONGENITAL AGAMMAGLOBULINEMIAPublished by American Academy of Pediatrics (AAP) ,1963