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Gwendoline Soler

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European Journal of Human Genetics : EJHG|May 29, 2002
Analysis of alterations of WFDC1, a new putative tumour suppressor gene, in hepatocellular carcinomaRaphaël Saffroy, Philippe Riou, Gwendoline Soler, et al.
Cancer Genetics and Cytogenetics|May 14, 2008
MLL insertion with MLL-MLLT3 gene fusion in acute leukemia: case report and review of the literatureGwendoline Soler, Isabelle Radford, Claus Meyer, et al.
Blood|June 19, 2010
NUP98-MLL fusion in human acute myeloblastic leukemiaSophie Kaltenbach, Gwendoline Soler, Carole Barin, et al.
Fetal Diagnosis and Therapy|February 4, 2012
Proportion of parents agreeing to delay fetal karyotyping until the third trimester of pregnancy in cases with an indicationJérôme Toutain, Marie-Anne Lemaire-Coustel, Marianne Begorre, et al.
Cancers|April 13, 2023
Optical Genome Mapping in Routine Cytogenetic Diagnosis of Acute LeukemiaGwendoline Soler, Zangbéwendé Guy Ouedraogo, Carole Goumy, et al.
Blood|April 9, 2011
Identification of a transforming MYB-GATA1 fusion gene in acute basophilic leukemia: a new entity in male infantsCathy Quelen, Eric Lippert, Stephanie Struski, et al.
Blood|July 5, 2007
Prognostic and oncogenic relevance of TLX1/HOX11 expression level in T-ALLsJulie Bergeron, Emmanuelle Clappier, Isabelle Radford, et al.
Diagnostics (Basel, Switzerland)|December 9, 2023
Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy TerminationCarole Goumy, Zangbéwendé Guy Ouedraogo, Elodie Bellemonte, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowthValérie Malan, Suzanne Chevallier, Gwendoline Soler, et al.
Haematologica|November 8, 2011
Functional analysis of the NUP98-CCDC28A fusion proteinArnaud Petit, Christine Ragu, Gwendoline Soler, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
European Journal of Human Genetics : EJHG|May 29, 2002
Analysis of alterations of WFDC1, a new putative tumour suppressor gene, in hepatocellular carcinomaRaphaël Saffroy, Philippe Riou, Gwendoline Soler, et al.
Cancer Genetics and Cytogenetics|May 14, 2008
MLL insertion with MLL-MLLT3 gene fusion in acute leukemia: case report and review of the literatureGwendoline Soler, Isabelle Radford, Claus Meyer, et al.
Blood|June 19, 2010
NUP98-MLL fusion in human acute myeloblastic leukemiaSophie Kaltenbach, Gwendoline Soler, Carole Barin, et al.
Fetal Diagnosis and Therapy|February 4, 2012
Proportion of parents agreeing to delay fetal karyotyping until the third trimester of pregnancy in cases with an indicationJérôme Toutain, Marie-Anne Lemaire-Coustel, Marianne Begorre, et al.
Cancers|April 13, 2023
Optical Genome Mapping in Routine Cytogenetic Diagnosis of Acute LeukemiaGwendoline Soler, Zangbéwendé Guy Ouedraogo, Carole Goumy, et al.
Blood|April 9, 2011
Identification of a transforming MYB-GATA1 fusion gene in acute basophilic leukemia: a new entity in male infantsCathy Quelen, Eric Lippert, Stephanie Struski, et al.
Blood|July 5, 2007
Prognostic and oncogenic relevance of TLX1/HOX11 expression level in T-ALLsJulie Bergeron, Emmanuelle Clappier, Isabelle Radford, et al.
Diagnostics (Basel, Switzerland)|December 9, 2023
Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy TerminationCarole Goumy, Zangbéwendé Guy Ouedraogo, Elodie Bellemonte, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowthValérie Malan, Suzanne Chevallier, Gwendoline Soler, et al.
Haematologica|November 8, 2011
Functional analysis of the NUP98-CCDC28A fusion proteinArnaud Petit, Christine Ragu, Gwendoline Soler, et al.
Pageof 2