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L Guibaud

Showing results (81-90 of 88) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 4, 2006
[Idiopathic intrahepatic portosytemic shunts in 4 children]F Rouveyrol, M Meyer, J R Lusson, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 23, 2025
Prenatal evaluation, diagnosis and management of fetal corpus callosal abnormalities: international Delphi consensusR Corroenne, D Paladini, I Papastefanou, et al.
Neurology|November 15, 2006
High frequency of creatine deficiency syndromes in patients with unexplained mental retardationL Lion-François, D Cheillan, G Pitelet, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 8, 2005
Prenatal prognosis of congenital diaphragmatic hernia using magnetic resonance imaging measurement of fetal lung volumeG Gorincour, J Bouvenot, M G Mourot, et al.
Journal of Medical Genetics|July 10, 2007
Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal gangliaY Saillour, G Zanni, V Des Portes, et al.
Clinical Genetics|March 3, 2018
Unexpected diagnosis of a SHH nonsense variant causing a variable phenotype ranging from familial coloboma and Intellectual disability to isolated microcephalyA-L Bruel, J Thevenon, F Huet, et al.
Clinical Genetics|April 5, 2016
Refining the phenotypical and mutational spectrum of Taybi-Linder syndromeA Putoux, A Alqahtani, L Pinson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 1, 2018
De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathyF Tran Mau-Them, L Guibaud, L Duplomb, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 4, 2006
[Idiopathic intrahepatic portosytemic shunts in 4 children]F Rouveyrol, M Meyer, J R Lusson, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 23, 2025
Prenatal evaluation, diagnosis and management of fetal corpus callosal abnormalities: international Delphi consensusR Corroenne, D Paladini, I Papastefanou, et al.
Neurology|November 15, 2006
High frequency of creatine deficiency syndromes in patients with unexplained mental retardationL Lion-François, D Cheillan, G Pitelet, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 8, 2005
Prenatal prognosis of congenital diaphragmatic hernia using magnetic resonance imaging measurement of fetal lung volumeG Gorincour, J Bouvenot, M G Mourot, et al.
Journal of Medical Genetics|July 10, 2007
Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal gangliaY Saillour, G Zanni, V Des Portes, et al.
Clinical Genetics|March 3, 2018
Unexpected diagnosis of a SHH nonsense variant causing a variable phenotype ranging from familial coloboma and Intellectual disability to isolated microcephalyA-L Bruel, J Thevenon, F Huet, et al.
Clinical Genetics|April 5, 2016
Refining the phenotypical and mutational spectrum of Taybi-Linder syndromeA Putoux, A Alqahtani, L Pinson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 1, 2018
De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathyF Tran Mau-Them, L Guibaud, L Duplomb, et al.
Pageof 9