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D Cherif

Showing results (21-30 of 39) with videos related to

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Leukemia|April 1, 1994
Hunting 11q23 deletions with fluorescence in situ hybridization (FISH)D Cherif, O Bernard, S Paulien, et al.
Genes, Chromosomes & Cancer|October 1, 1993
In situ hybridization to interphase nuclei in acute leukemiaS P Romana, D Cherif, M Le Coniat, et al.
Human Molecular Genetics|November 1, 1992
Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophyI Richard, O Broux, D Hillaire, et al.
Diabetes|October 1, 1995
Cloning, functional expression, and chromosomal localization of the human pancreatic islet glucose-dependent insulinotropic polypeptide receptorS Gremlich, A Porret, E H Hani, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|July 1, 1993
A novel translocation, t(9;11)(q33;q23) involving the HRX gene in an acute monocytic leukemiaM Le Coniat, S P Romana, O Bernard, et al.
Genomics|December 1, 1994
Large human YACs constructed in a rad52 strain show a reduced rate of chimerismM Haldi, V Perrot, M Saumier, et al.
Blood|April 1, 1995
A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet alpha-granules and chromosome 11 deletion at 11q23J Breton-Gorius, R Favier, J Guichard, et al.
Genes, Chromosomes & Cancer|January 1, 1990
Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemiasO Bernard, P Guglielmi, P Jonveaux, et al.
Leukemia|February 13, 2002
Translocation t(5;14)(q35;q32) in three cases of childhood T cell acute lymphoblastic leukemia: a new recurring and cryptic abnormalityC Hélias, V Leymarie, N Entz-Werle, et al.
Genomics|July 15, 1994
Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneityM Medhioub, D Cherif, F Benessy, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Leukemia|April 1, 1994
Hunting 11q23 deletions with fluorescence in situ hybridization (FISH)D Cherif, O Bernard, S Paulien, et al.
Genes, Chromosomes & Cancer|October 1, 1993
In situ hybridization to interphase nuclei in acute leukemiaS P Romana, D Cherif, M Le Coniat, et al.
Human Molecular Genetics|November 1, 1992
Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophyI Richard, O Broux, D Hillaire, et al.
Diabetes|October 1, 1995
Cloning, functional expression, and chromosomal localization of the human pancreatic islet glucose-dependent insulinotropic polypeptide receptorS Gremlich, A Porret, E H Hani, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|July 1, 1993
A novel translocation, t(9;11)(q33;q23) involving the HRX gene in an acute monocytic leukemiaM Le Coniat, S P Romana, O Bernard, et al.
Genomics|December 1, 1994
Large human YACs constructed in a rad52 strain show a reduced rate of chimerismM Haldi, V Perrot, M Saumier, et al.
Blood|April 1, 1995
A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet alpha-granules and chromosome 11 deletion at 11q23J Breton-Gorius, R Favier, J Guichard, et al.
Genes, Chromosomes & Cancer|January 1, 1990
Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemiasO Bernard, P Guglielmi, P Jonveaux, et al.
Leukemia|February 13, 2002
Translocation t(5;14)(q35;q32) in three cases of childhood T cell acute lymphoblastic leukemia: a new recurring and cryptic abnormalityC Hélias, V Leymarie, N Entz-Werle, et al.
Genomics|July 15, 1994
Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneityM Medhioub, D Cherif, F Benessy, et al.
Pageof 4