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Pathologie-Biologie|January 1, 1988
[The contribution of cytogenetics to the evaluation of residual disease in malignant hemopathies]M F Bertheas, J Fraisse, C Vasselon, et al.
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.
Therapie|November 1, 1993
[Pharmacokinetics of calcium antagonists]M O Richard
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.
Neuroreport|October 23, 1995
Methionine sulfoximine increases acetylcholine level in the rat brain: no relation with epileptogenesisO Richard, T Hevor
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.
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