Carrier detection in typical and atypical X-linked agammaglobulinemia

Ochs, 1980, Disorders of the B cell system, 239 Lederman, 1985, X-linked agammaglobulinemia: an analysis of 96 patients, Medicine, 64, 145, 10.1097/00005792-198505000-00001 Siegal, 1971, Lymphocytes in human immunodeficiency states: a study of membrane-associated immunoglobulins, Eur J Immunol, 1, 482, 10.1002/eji.1830010615 Cooper, 1972, Circulating B-cells in patients with immunodeficiency, Am J Pathol, 69, 513 Conley, 1985, B cells in patients with X-linked agammaglobulinemia, J Immunol, 134, 3070, 10.4049/jimmunol.134.5.3070 Pearl, 1978, B lymphocyte precursors in human bone marrow: an analysis of normal individuals and patients with antibody-deficiency states, J Immunol, 120, 1169, 10.4049/jimmunol.120.4.1169 Kwan, 1986, Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism, J Clin Invest, 77, 649, 10.1172/JCI112351 Mensink, 1986, Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity, Hum Genet, 73, 327, 10.1007/BF00279095 Malcolm, 1987, Close linkage of random DNA fragments from Xq 21.3–22 to X-linked agammaglobulinemia (XLA), Hum Genet, 77, 172, 10.1007/BF00272387 Hoffman, 1977, Hypoimmunoglobulinemia with normal T cell function in female siblings, Clin Immunol Immunopathol, 7, 364, 10.1016/0090-1229(77)90070-8 Buckley, 1968, Hereditary alterations in the immune response: coexistence of agammaglobulinemia, acquired hypoagammaglobulinemia and selective immunoglobulin deficiency in a sibship, Pediatr Res, 2, 72, 10.1203/00006450-196803000-00002 Goldblum, 1974, X-linked B lymphocyte deficiency. I. Panhypoglobulinemia and dysglobulinemia in siblings, J Pediatr, 85, 188, 10.1016/S0022-3476(74)80390-2 Leickley, 1986, Variability in B cell maturation and differentiation in X-linked agammaglobulinemia, Clin Exp Immunol, 65, 90 Landreth, 1985, Pre-B cells in agammaglobulinemia: evidence for disease heterogeneity among affected boys, J Clin Immunol, 5, 84, 10.1007/BF00915005 Fleisher, 1980, X-linked hypogammaglobulinemia and isolated growth hormone deficiency, N Engl J Med, 302, 1429, 10.1056/NEJM198006263022601 Conley, 1986, Expression of the gene defect in X-linked agammaglobulinemia, N Engl J Med, 315, 564, 10.1056/NEJM198608283150907 Fearon, 1987, Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation, N Engl J Med, 316, 427, 10.1056/NEJM198702193160802 Puck, 1987, Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation, J Clin Invest, 79, 1395, 10.1172/JCI112967 Migeon, 1972, Stability of X chromosomal inactivation in human somatic cells, Nature, 239, 87, 10.1038/239087a0 Conley, 1983, Serum IgA1 and IgA2 in normal adults and patients with systemic lupus erythematosus and hepatic disease, Clin Immunol Immunopathol, 26, 390, 10.1016/0090-1229(83)90123-X Conley, 1984, In vitro regulation of IgA subclass synthesis. II. The source of IgA2 plasma cells, J Immunol, 133, 2312, 10.4049/jimmunol.133.5.2312 Fuscoe, 1983, Deletion and amplification of the HPRT locus in Chinese hamster cells, J Mol Cell Biol, 3, 1086 Morton, 1955, Sequential tests for the detection of linkage, Am J Hum Genet, 7, 277 Fialkow, 1973, Primordial cell pool size and lineage relationships of five human cell types, Am Hum Genet, 37, 39, 10.1111/j.1469-1809.1973.tb01813.x Wyatt, 1973, Hypothesis: poliomyelitis in hypogammaglobulinemics, J Infect Dis, 128, 802, 10.1093/infdis/128.6.802 Wilfert, 1977, Persistent and fatal central-nervous-system echovirus infections in patients with agammaglobulinemia, N Engl J Med, 296, 1485, 10.1056/NEJM197706302962601