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M Pinard

Showing results (61-70 of 67) with videos related to

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BMC Musculoskeletal Disorders|March 12, 2022
Strategies aimed at preventing long-term opioid use in trauma and orthopaedic surgery: a scoping reviewC Côté, M Bérubé, L Moore, et al.
Cell|March 7, 1998
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndromeV des Portes, J M Pinard, P Billuart, et al.
Human Molecular Genetics|June 9, 1998
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)V des Portes, F Francis, J M Pinard, et al.
Journal of Medical Genetics|March 1, 1997
Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22V des Portes, J M Pinard, D Smadja, et al.
Neurology|August 1, 1996
X-linked malformations of neuronal migrationW B Dobyns, E Andermann, F Andermann, 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 Medical Genetics|May 7, 2013
Phenotype and genotype in 101 males with X-linked creatine transporter deficiencyJ M van de Kamp, O T Betsalel, S Mercimek-Mahmutoglu, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
BMC Musculoskeletal Disorders|March 12, 2022
Strategies aimed at preventing long-term opioid use in trauma and orthopaedic surgery: a scoping reviewC Côté, M Bérubé, L Moore, et al.
Cell|March 7, 1998
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndromeV des Portes, J M Pinard, P Billuart, et al.
Human Molecular Genetics|June 9, 1998
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)V des Portes, F Francis, J M Pinard, et al.
Journal of Medical Genetics|March 1, 1997
Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22V des Portes, J M Pinard, D Smadja, et al.
Neurology|August 1, 1996
X-linked malformations of neuronal migrationW B Dobyns, E Andermann, F Andermann, 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 Medical Genetics|May 7, 2013
Phenotype and genotype in 101 males with X-linked creatine transporter deficiencyJ M van de Kamp, O T Betsalel, S Mercimek-Mahmutoglu, et al.
Pageof 7