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Elise Boudry-Labis

Showing results (1-10 of 14) with videos related to

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Annales De Biologie Clinique|August 2, 2016
Cytogenetics in the management of "chronic myeloid leukemia": an update by the Groupe francophone de cytogénétique hématologique (GFCH)Catherine Roche-Lestienne, Elise Boudry-Labis, Marie-Joëlle Mozziconacci
Expert Review of Hematology|October 29, 2014
Prognosis and monitoring of core-binding factor acute myeloid leukemia: current and emerging factorsNicolas Duployez, Christophe Willekens, Alice Marceau-Renaut, et al.
European Journal of Human Genetics : EJHG|June 15, 2018
A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel-van der Aa syndromeMinh-Tuan Huynh, Elise Boudry-Labis, Alfred Massard, et al.
Clinical Case Reports|October 29, 2015
Diagnosis of intrachromosomal amplification of chromosome 21 (iAMP21) by molecular cytogenetics in pediatric acute lymphoblastic leukemiaNicolas Duployez, Elise Boudry-Labis, Gauthier Decool, et al.
European Journal of Medical Genetics|December 4, 2012
Split-hand/foot malformation with long-bone deficiency and BHLHA9 duplication: two cases and expansion of the phenotype to radial agenesisFlorence Petit, Joris Andrieux, Bénédicte Demeer, et al.
Neurogenetics|December 12, 2019
Neurodevelopmental phenotype associated with CHD8-SUPT16H duplicationThomas Smol, Caroline Thuillier, Elise Boudry-Labis, et al.
American Journal of Medical Genetics. Part A|April 12, 2017
WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletionMinh Tuan Huynh, Elise Boudry-Labis, Bénédicte Duban, et al.
Human Mutation|May 16, 2021
Dissection of contiguous gene effects for deletions around ERF on chromosome 19Eduardo Calpena, Simon J McGowan, Fiona Blanco Kelly, et al.
Oncotarget|February 22, 2018
SNP-array lesions in core binding factor acute myeloid leukemiaNicolas Duployez, Elise Boudry-Labis, Christophe Roumier, et al.
American Journal of Hematology|March 6, 2013
Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemiaElise Boudry-Labis, Catherine Roche-Lestienne, Olivier Nibourel, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Annales De Biologie Clinique|August 2, 2016
Cytogenetics in the management of "chronic myeloid leukemia": an update by the Groupe francophone de cytogénétique hématologique (GFCH)Catherine Roche-Lestienne, Elise Boudry-Labis, Marie-Joëlle Mozziconacci
Expert Review of Hematology|October 29, 2014
Prognosis and monitoring of core-binding factor acute myeloid leukemia: current and emerging factorsNicolas Duployez, Christophe Willekens, Alice Marceau-Renaut, et al.
European Journal of Human Genetics : EJHG|June 15, 2018
A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel-van der Aa syndromeMinh-Tuan Huynh, Elise Boudry-Labis, Alfred Massard, et al.
Clinical Case Reports|October 29, 2015
Diagnosis of intrachromosomal amplification of chromosome 21 (iAMP21) by molecular cytogenetics in pediatric acute lymphoblastic leukemiaNicolas Duployez, Elise Boudry-Labis, Gauthier Decool, et al.
European Journal of Medical Genetics|December 4, 2012
Split-hand/foot malformation with long-bone deficiency and BHLHA9 duplication: two cases and expansion of the phenotype to radial agenesisFlorence Petit, Joris Andrieux, Bénédicte Demeer, et al.
Neurogenetics|December 12, 2019
Neurodevelopmental phenotype associated with CHD8-SUPT16H duplicationThomas Smol, Caroline Thuillier, Elise Boudry-Labis, et al.
American Journal of Medical Genetics. Part A|April 12, 2017
WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletionMinh Tuan Huynh, Elise Boudry-Labis, Bénédicte Duban, et al.
Human Mutation|May 16, 2021
Dissection of contiguous gene effects for deletions around ERF on chromosome 19Eduardo Calpena, Simon J McGowan, Fiona Blanco Kelly, et al.
Oncotarget|February 22, 2018
SNP-array lesions in core binding factor acute myeloid leukemiaNicolas Duployez, Elise Boudry-Labis, Christophe Roumier, et al.
American Journal of Hematology|March 6, 2013
Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemiaElise Boudry-Labis, Catherine Roche-Lestienne, Olivier Nibourel, et al.
Pageof 2