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B Grandchamp

Showing results (51-60 of 134) with videos related to

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Human Genetics|December 1, 1995
Localization of the CDKN4/p27Kip1 gene to human chromosome 12p12.3E Martin, V Cacheux, H Cavé, et al.
Cytogenetics and Cell Genetics|August 18, 1999
Genomic organization of human JAK2 and mutation analysis of its JH2-domain in leukemiaJ Cools, P Peeters, T Voet, et al.
Human Genetics|April 1, 1995
A new mutation of the ALAS2 gene in a large family with X-linked sideroblastic anemiaE Prades, C Chambon, T A Dailey, et al.
Leukemia|December 22, 1999
Mapping of chromosome 20 for loss of heterozygosity in childhood ALL reveals a 1,000-kb deletion in one patientN Couque, C Chambon-Pautas, H Cavé, et al.
American Journal of Human Genetics|September 1, 1992
High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyriaX F Gu, F de Rooij, G Voortman, et al.
Human Genetics|August 1, 1991
Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyriaJ S Lee, G Lundin, L Lannfelt, et al.
British Journal of Haematology|July 1, 1997
Analysis of ETV6 and ETV6-AML1 proteins in acute lymphoblastic leukaemiaP Agape, B Gerard, H Cave, et al.
Clinical and Laboratory Haematology|April 25, 2001
Coinheritance of two alpha-spectrin gene defects in a recessive spherocytosis familyD Dhermy, J Steen-Johnsen, O Bournier, et al.
Human Genetics|November 1, 1994
Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12V Cacheux, P Martasek, F Fougerousse, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Recurrent molecular deletion of the 12p13 region, centromeric to ETV6/TEL, in T-cell prolymphocytic leukemiaG Hetet, H Dastot, M Baens, et al.
Pageof 14

Showing results (51-60 of 134) with videos related to

Sort By:
Pageof 14
Human Genetics|December 1, 1995
Localization of the CDKN4/p27Kip1 gene to human chromosome 12p12.3E Martin, V Cacheux, H Cavé, et al.
Cytogenetics and Cell Genetics|August 18, 1999
Genomic organization of human JAK2 and mutation analysis of its JH2-domain in leukemiaJ Cools, P Peeters, T Voet, et al.
Human Genetics|April 1, 1995
A new mutation of the ALAS2 gene in a large family with X-linked sideroblastic anemiaE Prades, C Chambon, T A Dailey, et al.
Leukemia|December 22, 1999
Mapping of chromosome 20 for loss of heterozygosity in childhood ALL reveals a 1,000-kb deletion in one patientN Couque, C Chambon-Pautas, H Cavé, et al.
American Journal of Human Genetics|September 1, 1992
High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyriaX F Gu, F de Rooij, G Voortman, et al.
Human Genetics|August 1, 1991
Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyriaJ S Lee, G Lundin, L Lannfelt, et al.
British Journal of Haematology|July 1, 1997
Analysis of ETV6 and ETV6-AML1 proteins in acute lymphoblastic leukaemiaP Agape, B Gerard, H Cave, et al.
Clinical and Laboratory Haematology|April 25, 2001
Coinheritance of two alpha-spectrin gene defects in a recessive spherocytosis familyD Dhermy, J Steen-Johnsen, O Bournier, et al.
Human Genetics|November 1, 1994
Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12V Cacheux, P Martasek, F Fougerousse, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Recurrent molecular deletion of the 12p13 region, centromeric to ETV6/TEL, in T-cell prolymphocytic leukemiaG Hetet, H Dastot, M Baens, et al.
Pageof 14