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V Des Portes

Showing results (31-40 of 59) with videos related to

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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 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.
Pathologie-Biologie|January 14, 1999
Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardationP Billuart, T Bienvenu, N Ronce, 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.
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.
Neurology|August 18, 2010
Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorderL Lion-Francois, C Mignot, S Vicart, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
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 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.
Pathologie-Biologie|January 14, 1999
Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardationP Billuart, T Bienvenu, N Ronce, 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.
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.
Neurology|August 18, 2010
Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorderL Lion-Francois, C Mignot, S Vicart, et al.
Pageof 6