X chromosome inactivation patterns in obligate carriers of X-linked lymphoproliferative syndrome
Open Access
- 1 June 1990
- journal article
- research article
- Published by Elsevier in Clinical Immunology and Immunopathology
- Vol. 55 (3), 486-491
- https://doi.org/10.1016/0090-1229(90)90133-b
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37Human Genetics, 1989
- Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on XqHuman Genetics, 1989
- Carrier detection in the Wiskott Aldrich syndromeBlood, 1988
- Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation.Journal of Clinical Investigation, 1987
- Epstein-Barr Virus Infections in Males with the X-Linked Lymphoproliterative SyndromeAnnals of Internal Medicine, 1987
- Expression of the Gene Defect in X-Linked AgammaglobulinemiaNew England Journal of Medicine, 1986
- X-linked lymphoproliferative syndrome. Natural history of the immunodeficiency.Journal of Clinical Investigation, 1983
- IMMUNOLOGICAL OBSERVATIONS ON PATENTS WITH LESCH-NYHAN SYNDROME, AND ON THE ROLE OF DE-NOVO PURINE SYNTHESIS IN LYMPHOCYTE TRANSFORMATIONThe Lancet, 1975
- Primordial cell pool size and lineage relationships of five human cell types*Annals of Human Genetics, 1973
- Absence of mosaicism in the lymphocyte in X-linked congenital hyperuricosuriaLife Sciences, 1968