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Showing results (21-30 of 27) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 20, 2007
[Revelation of an acute lymphoblastic leukemia in the delivery room]A Jacquot, F Bernard, M Dupont, et al.
European Journal of Biochemistry|May 12, 2000
ARP3beta, the gene encoding a new human actin-related protein, is alternatively spliced and predominantly expressed in brain neuronal cellsP Jay, J L Bergé-Lefranc, A Massacrier, et al.
American Journal of Medical Genetics|March 13, 1995
Heterotaxia syndrome and autosomal dominant inheritanceS Alonso, M E Pierpont, W Radtke, et al.
Human Reproduction (Oxford, England)|October 23, 2014
Discordant sex in monozygotic XXY/XX twins: a case reportG Tachon, G Lefort, J Puechberty, et al.
Nature Genetics|November 14, 1997
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal regionP Jay, C Rougeulle, A Massacrier, et al.
Leukemia|October 17, 2008
Heterogeneous patterns of amplification of the NUP214-ABL1 fusion gene in T-cell acute lymphoblastic leukemiaC Graux, M Stevens-Kroef, M Lafage, et al.
Leukemia|September 13, 2003
t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH)R Berger, N Dastugue, M Busson, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 20, 2007
[Revelation of an acute lymphoblastic leukemia in the delivery room]A Jacquot, F Bernard, M Dupont, et al.
European Journal of Biochemistry|May 12, 2000
ARP3beta, the gene encoding a new human actin-related protein, is alternatively spliced and predominantly expressed in brain neuronal cellsP Jay, J L Bergé-Lefranc, A Massacrier, et al.
American Journal of Medical Genetics|March 13, 1995
Heterotaxia syndrome and autosomal dominant inheritanceS Alonso, M E Pierpont, W Radtke, et al.
Human Reproduction (Oxford, England)|October 23, 2014
Discordant sex in monozygotic XXY/XX twins: a case reportG Tachon, G Lefort, J Puechberty, et al.
Nature Genetics|November 14, 1997
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal regionP Jay, C Rougeulle, A Massacrier, et al.
Leukemia|October 17, 2008
Heterogeneous patterns of amplification of the NUP214-ABL1 fusion gene in T-cell acute lymphoblastic leukemiaC Graux, M Stevens-Kroef, M Lafage, et al.
Leukemia|September 13, 2003
t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH)R Berger, N Dastugue, M Busson, et al.
Pageof 3