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M L Moutard

Showing results (31-40 of 45) with videos related to

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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 17, 2015
Prenatal features of isolated subependymal pseudocysts associated with adverse pregnancy outcomeH Esteban, E Blondiaux, E Audureau, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|November 14, 2015
[Preliminary results from the French study on prenatal repair for fetal myelomeningoceles (the PRIUM study)]S Friszer, F Dhombres, F Di Rocco, et al.
Clinical Genetics|June 4, 1998
Inherited microdeletion in Xp21.3-22.1 involved in non-specific mental retardationV des Portes, A Carrié, P Billuart, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 2, 2010
[Impact of prenatal corpus callosum agenesis diagnosis on pregnancy outcome. Evaluation of 155 cases between 2000 and 2006]A Isapof, V Kieffer, S Sacco, et al.
Human Molecular Genetics|July 1, 1996
Identification by STS PCR screening of a microdeletion in Xp21.3-22.1 associated with non-specific mental retardationP Billuart, M C Vinet, V des Portes, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 5, 2013
Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosisM Massoud, M Cagneaux, C Garel, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 10, 2020
Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesionsP Maurice, L Guilbaud, J Garel, 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.
AJNR. American Journal of Neuroradiology|December 24, 2021
Feasibility and Added Value of Fetal DTI Tractography in the Evaluation of an Isolated Short Corpus Callosum: Preliminary ResultsA-E Millischer, D Grevent, P Sonigo, 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.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 17, 2015
Prenatal features of isolated subependymal pseudocysts associated with adverse pregnancy outcomeH Esteban, E Blondiaux, E Audureau, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|November 14, 2015
[Preliminary results from the French study on prenatal repair for fetal myelomeningoceles (the PRIUM study)]S Friszer, F Dhombres, F Di Rocco, et al.
Clinical Genetics|June 4, 1998
Inherited microdeletion in Xp21.3-22.1 involved in non-specific mental retardationV des Portes, A Carrié, P Billuart, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 2, 2010
[Impact of prenatal corpus callosum agenesis diagnosis on pregnancy outcome. Evaluation of 155 cases between 2000 and 2006]A Isapof, V Kieffer, S Sacco, et al.
Human Molecular Genetics|July 1, 1996
Identification by STS PCR screening of a microdeletion in Xp21.3-22.1 associated with non-specific mental retardationP Billuart, M C Vinet, V des Portes, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 5, 2013
Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosisM Massoud, M Cagneaux, C Garel, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 10, 2020
Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesionsP Maurice, L Guilbaud, J Garel, 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.
AJNR. American Journal of Neuroradiology|December 24, 2021
Feasibility and Added Value of Fetal DTI Tractography in the Evaluation of an Isolated Short Corpus Callosum: Preliminary ResultsA-E Millischer, D Grevent, P Sonigo, 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.
Pageof 5