Mapping of the x-linked form of hyper-IgM syndrome (HIGM1) to Xq26 by close linkage to HPRT
- 31 October 1992
- Vol. 14 (2) , 551-553
- https://doi.org/10.1016/s0888-7543(05)80270-8
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Report of the committee on the genetic constitution of the X chromosome (Part 1 of 7)Cytogenetic and Genome Research, 1991
- Evidence that in X‐linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intactEuropean Journal of Immunology, 1990
- Close linkage of random DNA fragments from Xq 21.3–22 to X-linked agammaglobulinaemia (XLA)Human Genetics, 1987
- Evidence for a Defect in Switch T Cells in Patients with Immunodeficiency and Hyperimmunoglobulinemia MNew England Journal of Medicine, 1986
- Hyper Immunoglobulin M Immunodeficiency (Dysgammaglobulinemia)Journal of Clinical Investigation, 1979
- RECURRENT BACTERIAL INFECTIONS AND DYSGAMMAGLOBULINEMIA: DEFICIENCY OF 7S GAMMA-GLOBULINS IN THE PRESENCE OF ELEVATED 19S GAMMA-GLOBULINSPublished by American Academy of Pediatrics (AAP) ,1961