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Blood|January 1, 1995
A mutation located at the 5' splice junction sequence of intron 3 in the p67phox gene causes the lack of p67phox mRNA in a patient with chronic granulomatous diseaseL C Tanugi-Cholley, J P Issartel, J Lunardi, et al.Archives Francaises De Pediatrie|December 1, 1978
[Familial glomerulonephritis and hereditary deficiency of C2]C Genin, M T Freycon, F C Berthoux, et al.Revue D'Epidemiologie Et De Sante Publique|November 18, 2008
[Long term mortality of five-year survivors of childhood cancer in Rhône-Alpes region]B Trombert-Paviot, D Frappaz, L Casagranda, et al.Human Genetics|March 1, 1991
Genotype-phenotype relationship in various degrees of arylsulfatase A deficiencyJ Kappler, P Leinekugel, E Conzelmann, et al.Pediatrie|January 1, 1992
[Multifocal tuberculosis with cerebellar tuberculoma]D Frappaz, J Huppert, M H Deleage, et al.Cancer Genetics and Cytogenetics|February 1, 1986
Persistence of t(4;11) in cytologically normal bone marrow treated ex vivo with Asta-ZM F Bertheas, D Frappaz, J Fraisse, et al.British Journal of Cancer|May 1, 1982
Burkitt-type lymphoma in France among non-Hodgkin malignant lymphomas in Caucasian childrenT Philip, G M Lenoir, P A Bryon, et al.British Journal of Haematology|February 1, 1987
Effective multiagent chemotherapy in children with advanced B-cell lymphoma: who remains the high risk patient?T Philip, R Pinkerton, P Biron, et al.Pathologie-Biologie|September 1, 1986
[Chromosome polymorphism in allogeneic bone marrow grafts. Methods and results]M F Berthéas, D Frappaz, B Mascret, et al.Annales De Pediatrie|September 1, 1993
[Klinefelter syndrome in 1993. Results of a multicenter study on 58 cases and review of the literature]J Battin, G Malpuech, J L Nivelon, et al.Pageof 7