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L Villard

Showing results (81-90 of 99) with videos related to

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Physical Review Letters|June 13, 2009
Role of plasma elongation on turbulent transport in magnetically confined plasmasP Angelino, X Garbet, L Villard, et al.
Journal of Medical Genetics|July 4, 2001
Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the diseaseL Villard, N Lévy, F Xiang, et al.
Human Molecular Genetics|May 18, 2000
MECP2 mutations account for most cases of typical forms of Rett syndromeT Bienvenu, A Carrié, N de Roux, et al.
Neuropathology and Applied Neurobiology|May 11, 2017
In utero seizures revealing dentato-olivary dysplasia caused by SCN2A mutationF Sauvestre, S Moutton, C Badens, et al.
European Journal of Medical Genetics|February 14, 2006
Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular updateC Philippe, L Villard, N De Roux, et al.
European Journal of Human Genetics : EJHG|April 11, 2000
Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28L Villard, V des Portes, N Levy, et al.
Journal of Medical Genetics|October 21, 1999
Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1L Villard, S Briault, A M Lossi, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 19, 2025
Poor Association Between Clinical Characteristics and Seropositivity in Children With Suspected Long COVID-A Single-Centre StudyS Olsson-Åkefeldt, J Luthander, L Anmyr, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|November 27, 2002
[Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients]S G Vorsanova, V Iu Ulas, Iu B Iurov, et al.
American Journal of Medical Genetics|November 15, 2000
Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?S Briault, L Villard, U Rogner, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Physical Review Letters|June 13, 2009
Role of plasma elongation on turbulent transport in magnetically confined plasmasP Angelino, X Garbet, L Villard, et al.
Journal of Medical Genetics|July 4, 2001
Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the diseaseL Villard, N Lévy, F Xiang, et al.
Human Molecular Genetics|May 18, 2000
MECP2 mutations account for most cases of typical forms of Rett syndromeT Bienvenu, A Carrié, N de Roux, et al.
Neuropathology and Applied Neurobiology|May 11, 2017
In utero seizures revealing dentato-olivary dysplasia caused by SCN2A mutationF Sauvestre, S Moutton, C Badens, et al.
European Journal of Medical Genetics|February 14, 2006
Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular updateC Philippe, L Villard, N De Roux, et al.
European Journal of Human Genetics : EJHG|April 11, 2000
Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28L Villard, V des Portes, N Levy, et al.
Journal of Medical Genetics|October 21, 1999
Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1L Villard, S Briault, A M Lossi, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 19, 2025
Poor Association Between Clinical Characteristics and Seropositivity in Children With Suspected Long COVID-A Single-Centre StudyS Olsson-Åkefeldt, J Luthander, L Anmyr, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|November 27, 2002
[Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients]S G Vorsanova, V Iu Ulas, Iu B Iurov, et al.
American Journal of Medical Genetics|November 15, 2000
Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?S Briault, L Villard, U Rogner, et al.
Pageof 10