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J Nectoux

Showing results (21-30 of 26) with videos related to

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Neurology. Genetics|October 22, 2016
Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T)S T Oestergaard, T Stojkovic, J R Dahlqvist, et al.
International Journal of Cancer|February 20, 1991
Temporal change in diagnostic criteria as a cause of the increase of malignant melanoma over time is unlikelyE P van der Esch, C S Muir, J Nectoux, et al.
Journal of Medical Genetics|November 13, 2007
Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathyH Rosas-Vargas, N Bahi-Buisson, C Philippe, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 8, 2018
Performance of semiconductor sequencing platform for non-invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical settingL Allach El Khattabi, S Brun, P Gueguen, et al.
Journal of Medical Genetics|July 7, 2009
Novel FOXG1 mutations associated with the congenital variant of Rett syndromeM A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.
Muscle & Nerve|April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort StudyAlexandre Guérémy, V Morel, T Stojkovic, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Neurology. Genetics|October 22, 2016
Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T)S T Oestergaard, T Stojkovic, J R Dahlqvist, et al.
International Journal of Cancer|February 20, 1991
Temporal change in diagnostic criteria as a cause of the increase of malignant melanoma over time is unlikelyE P van der Esch, C S Muir, J Nectoux, et al.
Journal of Medical Genetics|November 13, 2007
Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathyH Rosas-Vargas, N Bahi-Buisson, C Philippe, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 8, 2018
Performance of semiconductor sequencing platform for non-invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical settingL Allach El Khattabi, S Brun, P Gueguen, et al.
Journal of Medical Genetics|July 7, 2009
Novel FOXG1 mutations associated with the congenital variant of Rett syndromeM A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.
Muscle & Nerve|April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort StudyAlexandre Guérémy, V Morel, T Stojkovic, et al.
Pageof 3