Carrier detection in typical and atypical X-linked agammaglobulinemia
Authors:
- Jennifer M. PuckJPJennifer M. Puck
Open Access
- 1 May 1988
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 112 (5) , 688-694
Abstract
No abstract availableKeywords
Funding Information
- March of Dimes Foundation (1077)
- Immune Deficiency Foundation
- National Institutes of Health (A1-21477, A1-25129, HD-00657)
This publication has 21 references indexed in Scilit:
- Carrier Detection in X-Linked Agammaglobulinemia by Analysis of X-Chromosome InactivationNew England Journal of Medicine, 1987
- Expression of the Gene Defect in X-Linked AgammaglobulinemiaNew England Journal of Medicine, 1986
- X-Linked AgammaglobulinemiaMedicine, 1985
- Serum IgA1 and IgA2 in normal adults and patients with systemic lupus erythematosus and hepatic diseaseClinical Immunology and Immunopathology, 1983
- X-Linked Hypogammaglobulinemia and Isolated Growth Hormone DeficiencyNew England Journal of Medicine, 1980
- Persistent and Fatal Central-Nervous-System ECHOvirus Infections in Patients with AgammaglobulinemiaNew England Journal of Medicine, 1977
- Hypoimmunoglobulinemia with normal T cell function in female siblingsClinical Immunology and Immunopathology, 1977
- X-linked B lymphocyte deficiencyThe Journal of Pediatrics, 1974
- Poliomyelitis in HypogammaglobulinemicsThe Journal of Infectious Diseases, 1973
- Stability of X Chromosomal Inactivation in Human Somatic CellsNature, 1972