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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.
European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 26, 2012
[Medical care of brain malformative vascular diseases discovered during the pre- or neonatal period]M Sachet, M Tardieu, P Durand, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 9, 2020
E.U. paediatric MOG consortium consensus: Part 1 - Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disordersArlette L Bruijstens, Christian Lechner, Lorraine Flet-Berliac, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 13, 2020
E.U. paediatric MOG consortium consensus: Part 4 - Outcome of paediatric myelin oligodendrocyte glycoprotein antibody-associated disordersArlette L Bruijstens, Markus Breu, Eva-Maria Wendel, et al.
Nature Genetics|November 4, 2000
Mutant WD-repeat protein in triple-A syndromeA Tullio-Pelet, R Salomon, S Hadj-Rabia, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 26, 2019
Prognostic value of diffusion-weighted magnetic resonance imaging of brain in fetal growth restriction: results of prospective multicenter studyJ M Jouannic, E Blondiaux, M V Senat, et al.
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