V des Portes - JoVE Visualize

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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 24, 2008

Abnormal Sylvian fissure on prenatal cerebral imaging: significance and correlation with neuropathological and postnatal dataL Guibaud, L Selleret, J C Larroche, et al.

Seizure|May 25, 2002

So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutationV des Portes, L Abaoub, A Joannard, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 3, 2015

[Smith-Magenis syndrome is an association of behavioral and sleep/wake circadian rhythm disorders]A Poisson, A Nicolas, D Sanlaville, et al.

Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 4, 2013

Distortion of the anterior part of the interhemispheric fissure: significance and implications for prenatal diagnosisN Vinurel, A Van Nieuwenhuyse, M Cagneaux, et al.

American Journal of Human Genetics|April 1, 1997

A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.

American Journal of Medical Genetics|October 23, 1997

Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, 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.

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.

Neuropediatrics|September 10, 1999

Subcortical laminar heterotopia in two sisters and their mother: MRI, clinical findings and pathogenesisP H van der Valk, I Snoeck, L C Meiners, 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.

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Showing results (21-30 of 48) 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|June 24, 2008

Abnormal Sylvian fissure on prenatal cerebral imaging: significance and correlation with neuropathological and postnatal dataL Guibaud, L Selleret, J C Larroche, et al.

Seizure|May 25, 2002

So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutationV des Portes, L Abaoub, A Joannard, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 3, 2015

[Smith-Magenis syndrome is an association of behavioral and sleep/wake circadian rhythm disorders]A Poisson, A Nicolas, D Sanlaville, et al.

Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 4, 2013

Distortion of the anterior part of the interhemispheric fissure: significance and implications for prenatal diagnosisN Vinurel, A Van Nieuwenhuyse, M Cagneaux, et al.

American Journal of Human Genetics|April 1, 1997

A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.

American Journal of Medical Genetics|October 23, 1997

Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, 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.

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.

Neuropediatrics|September 10, 1999

Subcortical laminar heterotopia in two sisters and their mother: MRI, clinical findings and pathogenesisP H van der Valk, I Snoeck, L C Meiners, 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.

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