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Cytogenetics and Cell Genetics|July 7, 1999
Abnormal methylation does not prevent X inactivation in ICF patientsD Bourc'his, P Miniou, M Jeanpierre, et al.The Journal of Clinical Investigation|April 1, 1991
Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome)G de Saint-Basile, F Le Deist, J P de Villartay, et al.Neurology|March 17, 2012
CNS involvement at the onset of primary hemophagocytic lymphohistiocytosisK Deiva, N Mahlaoui, F Beaudonnet, et al.Archives Francaises De Pediatrie|December 1, 1985
[Complications of the prolonged use of lipid emulsion in children on parenteral nutrition]O Goulet, R Girot, M Maier-Redelsperger, et al.Journal of Immunology (Baltimore, Md. : 1950)|February 15, 1995
Undetectable CD40 ligand expression on T cells and low B cell responses to CD40 binding agonists in human newbornsA Durandy, G De Saint Basile, B Lisowska-Grospierre, et al.The Journal of Pediatrics|October 1, 1993
Severe combined immunodeficiency: a retrospective single-center study of clinical presentation and outcome in 117 patientsJ L Stephan, V Vlekova, F Le Deist, et al.Human Genetics|May 1, 1992
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 betaG de Saint Basile, L D Notarangelo, C Bonaiti-Pellié, et al.Genomics|March 8, 2000
Two genes are responsible for Griscelli syndrome at the same 15q21 locusE Pastural, F Ersoy, N Yalman, et al.American Journal of Medical Genetics|April 1, 1992
Congenital X-linked ataxia, progressive myoclonic encephalopathy, macular degeneration and recurrent infectionsE Bertini, R Cusmai, G de Saint Basile, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1987
Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13G de Saint Basile, B Arveiler, I Oberlé, et al.Pageof 9