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Fabien Guimiot

Showing results (51-60 of 92) with videos related to

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American Journal of Medical Genetics. Part A|November 26, 2009
Abnormal muscle development of the diaphragm in a fetus with 2p14-p16 duplicationRomain Guilherme, Fabien Guimiot, Anne-Claude Tabet, et al.
European Journal of Medical Genetics|July 20, 2021
Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndromeNina-Maria Wilpert, Florent Marguet, Camille Maillard, et al.
Frontiers in Immunology|December 17, 2020
CD4<sup>+</sup>CD8<sup>+</sup> T-Lymphocytes in Xenogeneic and Human Graft-versus-Host DiseaseKutaiba Alhaj Hussen, David Michonneau, Vincent Biajoux, et al.
Gynecologic and Obstetric Investigation|November 1, 2018
Three-Dimensional Modelization of the Female Human Inferior Hypogastric Plexus: Implications for Nerve-Sparing Radical HysterectomyVincent Balaya, Fabien Guimiot, Jean-François Uhl, et al.
Molecular Syndromology|August 25, 2018
Severe Phenotype of Cutis Laxa Type 1B with Antenatal Signs due to a Novel Homozygous Nonsense Mutation in <i>EFEMP2</i>Pascaline Letard, Dorien Schepers, Juliette Albuisson, et al.
The Journal of Clinical Endocrinology and Metabolism|November 2, 2006
Sodium/iodide symporter (NIS) gene expression is the limiting step for the onset of thyroid function in the human fetusGabor Szinnai, Ludovic Lacroix, Aurore Carré, et al.
Medrxiv : the Preprint Server for Health Sciences|September 10, 2024
New <i>ZNHIT3</i> Variants Disrupting snoRNP Assembly Cause Prenatal PEHO Syndrome with Isolated HydropsMd Lutfur Rahman, Adeline A Bonnard, Feng Wang, et al.
Molecular Cytogenetics|October 17, 2014
3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndromeCeline Dupont, Martine Bucourt, Fabien Guimiot, et al.
Hemasphere|March 26, 2025
Two distinct fetal-type signatures characterize juvenile myelomonocytic leukemiaMarion Strullu, Chloé Arfeuille, Aurélie Caye-Eude, et al.
American Journal of Medical Genetics. Part A|June 3, 2017
Molecular and clinical delineation of 2p15p16.1 microdeletion syndromeJonathan Lévy, Aurélie Coussement, Céline Dupont, et al.
Pageof 10

Showing results (51-60 of 92) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics. Part A|November 26, 2009
Abnormal muscle development of the diaphragm in a fetus with 2p14-p16 duplicationRomain Guilherme, Fabien Guimiot, Anne-Claude Tabet, et al.
European Journal of Medical Genetics|July 20, 2021
Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndromeNina-Maria Wilpert, Florent Marguet, Camille Maillard, et al.
Frontiers in Immunology|December 17, 2020
CD4<sup>+</sup>CD8<sup>+</sup> T-Lymphocytes in Xenogeneic and Human Graft-versus-Host DiseaseKutaiba Alhaj Hussen, David Michonneau, Vincent Biajoux, et al.
Gynecologic and Obstetric Investigation|November 1, 2018
Three-Dimensional Modelization of the Female Human Inferior Hypogastric Plexus: Implications for Nerve-Sparing Radical HysterectomyVincent Balaya, Fabien Guimiot, Jean-François Uhl, et al.
Molecular Syndromology|August 25, 2018
Severe Phenotype of Cutis Laxa Type 1B with Antenatal Signs due to a Novel Homozygous Nonsense Mutation in <i>EFEMP2</i>Pascaline Letard, Dorien Schepers, Juliette Albuisson, et al.
The Journal of Clinical Endocrinology and Metabolism|November 2, 2006
Sodium/iodide symporter (NIS) gene expression is the limiting step for the onset of thyroid function in the human fetusGabor Szinnai, Ludovic Lacroix, Aurore Carré, et al.
Medrxiv : the Preprint Server for Health Sciences|September 10, 2024
New <i>ZNHIT3</i> Variants Disrupting snoRNP Assembly Cause Prenatal PEHO Syndrome with Isolated HydropsMd Lutfur Rahman, Adeline A Bonnard, Feng Wang, et al.
Molecular Cytogenetics|October 17, 2014
3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndromeCeline Dupont, Martine Bucourt, Fabien Guimiot, et al.
Hemasphere|March 26, 2025
Two distinct fetal-type signatures characterize juvenile myelomonocytic leukemiaMarion Strullu, Chloé Arfeuille, Aurélie Caye-Eude, et al.
American Journal of Medical Genetics. Part A|June 3, 2017
Molecular and clinical delineation of 2p15p16.1 microdeletion syndromeJonathan Lévy, Aurélie Coussement, Céline Dupont, et al.
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