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B Grandchamp

Showing results (101-110 of 134) with videos related to

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Leukemia|January 1, 1990
Detection of minimal residual disease in chronic myeloid leukemia patients after bone marrow transplantation by polymerase chain reactionM H Delfau, J P Kerckaert, M Collyn d'Hooghe, et al.
Human Genetics|January 1, 1984
Assignment of the gene for uroporphyrinogen decarboxylase to human chromosome 1 by somatic cell hybridization and specific enzyme immunoassayH de Verneuil, B Grandchamp, C Foubert, et al.
Leukemia|March 10, 2001
Deletion of chromosomal region 13q14.3 in childhood acute lymphoblastic leukemiaH Cavé, H Avet-Loiseau, I Devaux, et al.
British Journal of Haematology|December 1, 1992
Quantitative determination of the hybrid Bcr-Abl RNA in patients with chronic myelogenous leukaemia under interferon therapyM C Malinge, F X Mahon, M H Delfau, et al.
Clinical Chemistry|January 1, 1992
Denaturing gradient gel electrophoresis for rapid detection of latent carriers of a subtype of acute intermittent porphyria with normal erythrocyte porphobilinogen deaminase activityF Bourgeois, X F Gu, J C Deybach, et al.
European Journal of Clinical Investigation|October 1, 1989
Molecular analysis of acute intermittent porphyria in a Finnish family with normal erythrocyte porphobilinogen deaminaseB Grandchamp, C Picat, R Kauppinen, et al.
Clinical Chemistry|May 1, 1996
Fluorometric detection of HIV-1 genome through use of an internal control, inosine-substituted primers, and microtiter plate formatB Gérard, C Peponnet, G Brunie, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1989
[Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant]M Garbarz, I Devaux, B Grandchamp, et al.
Schizophrenia Research|January 1, 1993
Association between genetic variation at the porphobilinogen deaminase gene and schizophreniaA R Sanders, D E Rincon-Limas, R Chakraborty, et al.
Annales De Dermatologie Et De Venereologie|March 16, 2010
[Intra- and interfamilial phenotype variation in Birt-Hogg-Dubé syndrome: Consequences for therapy]M Steff, A Bourillon, T Frebourg, et al.
Pageof 14

Showing results (101-110 of 134) with videos related to

Sort By:
Pageof 14
Leukemia|January 1, 1990
Detection of minimal residual disease in chronic myeloid leukemia patients after bone marrow transplantation by polymerase chain reactionM H Delfau, J P Kerckaert, M Collyn d'Hooghe, et al.
Human Genetics|January 1, 1984
Assignment of the gene for uroporphyrinogen decarboxylase to human chromosome 1 by somatic cell hybridization and specific enzyme immunoassayH de Verneuil, B Grandchamp, C Foubert, et al.
Leukemia|March 10, 2001
Deletion of chromosomal region 13q14.3 in childhood acute lymphoblastic leukemiaH Cavé, H Avet-Loiseau, I Devaux, et al.
British Journal of Haematology|December 1, 1992
Quantitative determination of the hybrid Bcr-Abl RNA in patients with chronic myelogenous leukaemia under interferon therapyM C Malinge, F X Mahon, M H Delfau, et al.
Clinical Chemistry|January 1, 1992
Denaturing gradient gel electrophoresis for rapid detection of latent carriers of a subtype of acute intermittent porphyria with normal erythrocyte porphobilinogen deaminase activityF Bourgeois, X F Gu, J C Deybach, et al.
European Journal of Clinical Investigation|October 1, 1989
Molecular analysis of acute intermittent porphyria in a Finnish family with normal erythrocyte porphobilinogen deaminaseB Grandchamp, C Picat, R Kauppinen, et al.
Clinical Chemistry|May 1, 1996
Fluorometric detection of HIV-1 genome through use of an internal control, inosine-substituted primers, and microtiter plate formatB Gérard, C Peponnet, G Brunie, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1989
[Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant]M Garbarz, I Devaux, B Grandchamp, et al.
Schizophrenia Research|January 1, 1993
Association between genetic variation at the porphobilinogen deaminase gene and schizophreniaA R Sanders, D E Rincon-Limas, R Chakraborty, et al.
Annales De Dermatologie Et De Venereologie|March 16, 2010
[Intra- and interfamilial phenotype variation in Birt-Hogg-Dubé syndrome: Consequences for therapy]M Steff, A Bourillon, T Frebourg, et al.
Pageof 14