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Journal of Medical Genetics|January 15, 2013
Breakpoint mapping by next generation sequencing reveals causative gene disruption in patients carrying apparently balanced chromosome rearrangements with intellectual deficiency and/or congenital malformationsCaroline Schluth-Bolard, Audrey Labalme, Marie-Pierre Cordier, et al.American Journal of Medical Genetics. Part A|November 21, 2012
Mosaic 18q21.2 deletions including the TCF4 gene: a clinical reportMassimiliano Rossi, Audrey Labalme, Marie-Pierre Cordier, et al.Life Science Alliance|July 2, 2026
TERT drives liver tumorigenesis beyond telomere elongationLaura Braud, Julien Vernerey, Arnaud Guille, et al.Journal of Hepatology|November 26, 2025
Intratumour Ploidy Heterogeneity and Clonal Evolution in Hepatocellular CarcinomaPierre Cordier, Théo Z Hirsch, Stefano Caruso, et al.Pediatric Radiology|February 4, 2015
Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesisMassimiliano Rossi, Christine M Hall, Raymonde Bouvier, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 27, 2017
Outcome of isolated agenesis of the corpus callosum: A population-based prospective studyVincent des Portes, Anne Rolland, Juan Velazquez-Dominguez, et al.European Journal of Medical Genetics|February 19, 2013
Neuropathological features in a female fetus with OPHN1 deletion and cerebellar hypoplasiaDelphine Rocas, Eudeline Alix, Jessica Michel, et al.American Journal of Human Genetics|October 1, 2013
Recessive and dominant mutations in retinoic acid receptor beta in cases with microphthalmia and diaphragmatic herniaMyriam Srour, David Chitayat, Véronique Caron, et al.Oncoimmunology|July 26, 2023
Formyl peptide receptor-1 (FPR1) represses intestinal oncogenesisJulie Le Naour, Léa Montégut, Yuhong Pan, et al.Journal of Medical Genetics|September 1, 2010
BBS10 mutations are common in 'Meckel'-type cystic kidneysAudrey Putoux, Soumaya Mougou-Zerelli, Sophie Thomas, et al.Pageof 6