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Proceedings of the National Academy of Sciences of the United States of America|July 21, 1999
Defective CTLA-4 cycling pathway in Chediak-Higashi syndrome: a possible mechanism for deregulation of T lymphocyte activationF J Barrat, F Le Deist, M Benkerrou, et al.
The Journal of Clinical Investigation|March 1, 1993
Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiencyM Cavazzana-Calvo, F Le Deist, G De Saint Basile, et al.
Lancet (London, England)|December 2, 1989
Close linkage of hypervariable marker DXS255 to disease locus of Wiskott-Aldrich syndromeG de Saint Basile, B Arveiler, N J Fraser, et al.
Human Genetics|September 1, 1988
Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotypeG de Saint-Basile, M C Bohler, A Fischer, et al.
International Journal of Molecular Medicine|July 14, 1999
Genetic basis of hemophagocytic lymphohistiocytosis syndrome (Review)R Dufourcq-Lagelouse, E Pastural, F J Barrat, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1R Dufourcq-Lagelouse, N Lambert, M Duval, et al.
Blood|May 1, 1985
Enhanced plasminogen-activator production by leukocytes in the human and murine Chediak-Higashi syndromeG de Saint Basile, A Fischer, M D Dautzenberg, et al.
American Journal of Medical Genetics|July 15, 1992
Carrier detection and prenatal diagnosis of X-linked agammaglobulinemiaO Journet, A Durandy, M Doussau, et al.
European Journal of Immunology|September 6, 2001
Signaling lymphocytic activation molecule (SLAM) regulates T cellular cytotoxicityG Henning, M S Kraft, T Derfuss, et al.
Bulletin De L'Academie Nationale De Medecine|March 23, 2001
[Gene therapy for immune deficiencies]A Fischer, S Hacein-Bey, F Le Deist, et al.
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