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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 cells
P Jay, J L Bergé-Lefranc, A Massacrier, et al.
American Journal of Medical Genetics
|
March 13, 1995
Heterotaxia syndrome and autosomal dominant inheritance
S Alonso, M E Pierpont, W Radtke, et al.
Human Reproduction (Oxford, England)
|
October 23, 2014
Discordant sex in monozygotic XXY/XX twins: a case report
G 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 region
P 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 leukemia
C 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.
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of 3
Search research articles
Search
Showing results (21-30 of 27) with videos related to
Sort By:
Page
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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 cells
P Jay, J L Bergé-Lefranc, A Massacrier, et al.
American Journal of Medical Genetics
|
March 13, 1995
Heterotaxia syndrome and autosomal dominant inheritance
S Alonso, M E Pierpont, W Radtke, et al.
Human Reproduction (Oxford, England)
|
October 23, 2014
Discordant sex in monozygotic XXY/XX twins: a case report
G 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 region
P 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 leukemia
C 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.
Page
of 3