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Christophe Philippe

Showing results (21-30 of 150) with videos related to

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Therapeutic Advances in Psychopharmacology|December 7, 2020
Early labor force exits in patients with treatment-resistant depression: an assessment of work years lost in a Danish nationwide register-based cohort studyKathrine Bang Madsen, Liselotte Vogdrup Petersen, Oleguer Plana-Ripoll, et al.
American Journal of Medical Genetics. Part A|March 19, 2025
Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2 -Related Disorders to a Syndromic Multiple Tumor PhenotypeMarie Lucain, Antonio Vitobello, Bekim Sadikovic, et al.
American Journal of Medical Genetics. Part A|February 9, 2022
Expanding the phenotype of HNRNPU-related neurodevelopmental disorder with emphasis on seizure phenotype and review of literatureJames Taylor, Michael Spiller, Kara Ranguin, et al.
Journal of Medical Genetics|May 28, 2011
Microtriplication of 11q24.1: a highly recognisable phenotype with short stature, distinctive facial features, keratoconus, overweight, and intellectual disabilityClaire Beneteau, Emilie Landais, Martine Doco-Fenzy, et al.
Pediatric Neurology|August 12, 2009
Neurologic aspects of MECP2 gene duplication in male patientsBernard Echenne, Agathe Roubertie, Dorien Lugtenberg, et al.
European Journal of Medical Genetics|March 18, 2018
15q24.1 BP4-BP1 microdeletion unmasking paternally inherited functional polymorphisms combined with distal 15q24.2q24.3 duplication in a patient with epilepsy, psychomotor delay, overweight, ventricular arrhythmiaMinh-Tuan Huynh, Anne-Sophie Lambert, Lucie Tosca, et al.
Pediatric Neurology|May 2, 2006
The incidence of Rett syndrome in FranceThierry Bienvenu, Christophe Philippe, Nicolas De Roux, et al.
European Journal of Human Genetics : EJHG|February 21, 2013
Extended spectrum of MBD5 mutations in neurodevelopmental disordersCéline Bonnet, Asma Ali Khan, Emmanuel Bresso, et al.
Acta Psychiatrica Scandinavica|August 23, 2022
Genetic and psychosocial influence on the association between early childhood infections and later psychiatric disordersJean-Christophe Philippe Goldtsche Debost, Erla Thorsteinsson, Betina Trabjerg, et al.
Molecular Genetics & Genomic Medicine|April 16, 2025
First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van den Ende-Gupta and 22q11.2 Deletion SyndromesCaroline Racine, Aurore Garde, Olivia Martz, et al.
Pageof 15

Showing results (21-30 of 150) with videos related to

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Pageof 15
Therapeutic Advances in Psychopharmacology|December 7, 2020
Early labor force exits in patients with treatment-resistant depression: an assessment of work years lost in a Danish nationwide register-based cohort studyKathrine Bang Madsen, Liselotte Vogdrup Petersen, Oleguer Plana-Ripoll, et al.
American Journal of Medical Genetics. Part A|March 19, 2025
Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2 -Related Disorders to a Syndromic Multiple Tumor PhenotypeMarie Lucain, Antonio Vitobello, Bekim Sadikovic, et al.
American Journal of Medical Genetics. Part A|February 9, 2022
Expanding the phenotype of HNRNPU-related neurodevelopmental disorder with emphasis on seizure phenotype and review of literatureJames Taylor, Michael Spiller, Kara Ranguin, et al.
Journal of Medical Genetics|May 28, 2011
Microtriplication of 11q24.1: a highly recognisable phenotype with short stature, distinctive facial features, keratoconus, overweight, and intellectual disabilityClaire Beneteau, Emilie Landais, Martine Doco-Fenzy, et al.
Pediatric Neurology|August 12, 2009
Neurologic aspects of MECP2 gene duplication in male patientsBernard Echenne, Agathe Roubertie, Dorien Lugtenberg, et al.
European Journal of Medical Genetics|March 18, 2018
15q24.1 BP4-BP1 microdeletion unmasking paternally inherited functional polymorphisms combined with distal 15q24.2q24.3 duplication in a patient with epilepsy, psychomotor delay, overweight, ventricular arrhythmiaMinh-Tuan Huynh, Anne-Sophie Lambert, Lucie Tosca, et al.
Pediatric Neurology|May 2, 2006
The incidence of Rett syndrome in FranceThierry Bienvenu, Christophe Philippe, Nicolas De Roux, et al.
European Journal of Human Genetics : EJHG|February 21, 2013
Extended spectrum of MBD5 mutations in neurodevelopmental disordersCéline Bonnet, Asma Ali Khan, Emmanuel Bresso, et al.
Acta Psychiatrica Scandinavica|August 23, 2022
Genetic and psychosocial influence on the association between early childhood infections and later psychiatric disordersJean-Christophe Philippe Goldtsche Debost, Erla Thorsteinsson, Betina Trabjerg, et al.
Molecular Genetics & Genomic Medicine|April 16, 2025
First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van den Ende-Gupta and 22q11.2 Deletion SyndromesCaroline Racine, Aurore Garde, Olivia Martz, et al.
Pageof 15