X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings.

Report of the committee on the genetic constitution of the X chromosome (Part 1 of 3)

1990 • 597 citations

The rate of spontaneous mutation of a human gene

1935 • 510 citations

Transplantation for severe combined immunodeficiency with HLA-A,B,D,DR incompatible parental marrow cells fractionated by soybean agglutinin and sheep red blood cells

1983 • 497 citations

Clonal analysis using recombinant DNA probes from the X-chromosome.

1987 • 439 citations

X-Linked Agammaglobulinemia

1985 • 415 citations

Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-X

1988 • 275 citations

Development of immunity in human severe primary T cell deficiency following haploidentical bone marrow stem cell transplantation.

1986 • 199 citations

Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation.

1987 • 154 citations

Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency.

1988 • 125 citations

Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.

1987 • 108 citations

Thymic dysplasia (“Swiss agammaglobulinemia”)

1967 • 90 citations

Selective defect of precursor T cells associated with apparently normal B lymphocytes in severe combined immunodeficiency disease

1978 • 71 citations

Heterogeneity of lymphocyte subpopulations in severe combined immunodeficiency. Evidence against a stem cell defect.

1976 • 61 citations

Presence of plasma cells and gamma-1-M-globulin synthesis in a patient with thymic alymphoplasia.

1966 • 57 citations

Adenosine deaminase and purine nucleoside phosphorylase deficiencies: Evaluation of therapeutic interventions in eight patients

1987 • 54 citations

X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.

1989 • 51 citations

Diagnosis and classification of severe combined immunodeficiency disease.

1983 • 49 citations

Immunologic reconstitution after haploidentical bone marrow transplantation for immune deficiency disorders: treatment of bone marrow cells with monoclonal antibody CT-2 and complement

1987 • 46 citations

Genetic deficiencies of adenosine deaminase and purine nucleoside phosphorylase: overview, genetic heterogeneity and therapy.

1983 • 45 citations

XX T cells and XY B cells in two patients with severe combined immune deficiency

1984 • 27 citations

Thymic dysplasia (“Swiss agammaglobulinemia”)

1967 • 27 citations

Accelerated development of immunity following transplantation of maternal marrow stem cells into infants with severe combined immunodeficiency and transplacentally acquired lymphoid chimerism.

1988 • 25 citations

Transfer factor induced delayed hypersensitivity in X-linked combined immunodeficiency

1973 • 23 citations

Report of the committee on the genetic constitution of the X chromosome

1988 • 17 citations

[Disorders in blood coagulation].

1954 • 11 citations

Immunologic reconstitution after haploidentical bone marrow transplantation for immune deficiency disorders: treatment of bone marrow cells with monoclonal antibody CT-2 and complement

1987 • 4 citations