1. Gelfand EW, Dosch HM. Diagnosis and classification of severe combined immunodeficiency disease. Birth Defects. 1983;19:65-72.
2.
2. Conley ME. X-linked severe combined immunodeficiency. Clin Immunol Immunopathol1991;61:S94-S99.
3.
3. Hirshhom R. Inherited enzyme deficiencies and immunodeficiency: Adenosine deaminase (ADA) and purine nucleoside phosphorylase (PNP) deficiencies. Clin ImmunolImmunopathol. 1986;40:157-165.
4.
4. Touraine JL, Betuel H, Souillet G,Jeune M. Combined immunodeficiency disease associated with absence of cell surface HLA-A and-B antigens. J Pediatr. 1978;93:47-51.
5.
5. Arnaiz-Villena A, Timon M, Corell A, et al. Primary immunodeficiency caused by mutations in the gene encoding the CD3-y subunit of the T-lymphocyte receptor. N EnglJ Med. 1992; 327:529-533.
6.
6. Sleasman JW, Tedder TF, Barrett DJ. Combined immunodeficiency due to the selective absence of CD4 inducer T lymphocytes. Clin Immunol ImmunopathoL1990;55:401-417.
7.
7. Elder ME, Lin D, Clever J, et al. Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase. Science. 1994;264(5165): 1596-1599.
8.
8. Gatti RA, Platt P, Pomerance HH, et al. Hereditary lymphopenic agammaglobulinemia associated with a distinct form of short-limbed dwarfism and ectodermal dysplasia. JPediatr. 1969;75:675-684.
9.
9. Omenn GS. Familial reticuloendotheliosis with eosinophilia. N Engl J Med. 1965;273:427-432.
10.
10. DeVal OM. Reticular dysgenesis. Lancet. 1959;Dec:1123-1125.
11.
11. Leonard W. The defective gene in X-linked severe combined immunodeficiency encodes a shared interleukin receptor subunit: implications for cytokine pleiotropy and redundancy. Curr Opin ImmunoL1994;6:631-635.
12.
12. Sindel LJ, Buckley RH, Schiff SE, et al. Severe combined immunodeficiency with natural killer-cell predominance: abrogation of graft-versus-host disease and immunologic reconstruction with HILA-identical bone marrow cells. JAIl Clin Immunol. 1984;73:829-836.
13.
13. Wahn V,Yokota S, Meyer KL. Expansion of a maternally derived monoclonal T cell population with CD3+/CD8+/T cell receptor-gamma/delta+ phenotype in a child with severe combined immunodeficiency. J Immunol. 1991; 147(9):2934-2941.
14.
14. Thompson A, Hendriks RW. Severe combined immunodeficiency in a man with an absence of immunoglobulin gene rearrangements but normal T cell receptor assembly. Eur J Immunol. 1990;2051-2056.
15.
15. Stephan JL, Vlekova V, LeDeist F, et al. Severe combined immunodeficiency: A retrospective single-center study of clinical presentation and outcome in 117 patients. JPediatr. 1993;123:564-572.
16.
16. Bosma GC, Fried M, Custer RP, et al. Evidence of functional lymphocytes in some (leaky) SCID mice. J Exp Med. 1988;167:1016-1033.
17.
17. Weinberg K, Parkman R. Age, the thymus, and T lymphocytes. NEngljMed. 1995;332:182-183.