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L Villard

Showing results (91-100 of 99) with videos related to

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Journal of Pharmaceutical Sciences|February 15, 2001
New bis(SATE) prodrug of AZT 5'-monophosphate: in vitro anti-HIV activity, stability, and potential oral absorptionM Shafiee, S Deferme, A L Villard, et al.
Journal of Medical Genetics|April 16, 1999
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndromeL Villard, M C Bonino, F Abidi, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|August 25, 2005
[Epigenetic study of Rett's syndrome as an adequate model for autistic disorders]I Iu Iurov, S G Vorsanova, V Iu Voinova-Ulas, et al.
Human Genetics|September 12, 2000
Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardationM J Friez, F B Essop, A Krause, et al.
Neurology|December 17, 2008
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletionC Cardoso, A Boys, E Parrini, et al.
American Journal of Medical Genetics|April 20, 1999
Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997J J Holden, M Percy, D Allingham-Hawkins, 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.
Journal of Medical Genetics|August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutationsN Bahi-Buisson, K Poirier, N Boddaert, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2009
Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutationsG Solé, I Coupry, C Rooryck, et al.
Pageof 10

Showing results (91-100 of 99) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 99 results.
Journal of Pharmaceutical Sciences|February 15, 2001
New bis(SATE) prodrug of AZT 5'-monophosphate: in vitro anti-HIV activity, stability, and potential oral absorptionM Shafiee, S Deferme, A L Villard, et al.
Journal of Medical Genetics|April 16, 1999
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndromeL Villard, M C Bonino, F Abidi, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|August 25, 2005
[Epigenetic study of Rett's syndrome as an adequate model for autistic disorders]I Iu Iurov, S G Vorsanova, V Iu Voinova-Ulas, et al.
Human Genetics|September 12, 2000
Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardationM J Friez, F B Essop, A Krause, et al.
Neurology|December 17, 2008
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletionC Cardoso, A Boys, E Parrini, et al.
American Journal of Medical Genetics|April 20, 1999
Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997J J Holden, M Percy, D Allingham-Hawkins, 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.
Journal of Medical Genetics|August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutationsN Bahi-Buisson, K Poirier, N Boddaert, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2009
Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutationsG Solé, I Coupry, C Rooryck, et al.
Pageof 10