Usha Kini Oxford Radcliffe NHS Trust Biography Publications Institution JoVE Articles Usha Kini has not added a biography. If you are Usha Kini and would like to personalize this page please email our Author Liaison for assistance. Publications Mutations in PIGY: Expanding the Phenotype of Inherited Glycosylphosphatidylinositol Deficiencies Human Molecular Genetics. Nov, 2015 | Pubmed ID: 26293662 Germline Recessive Mutations in PI4KA Are Associated with Perisylvian Polymicrogyria, Cerebellar Hypoplasia and Arthrogryposis Human Molecular Genetics. Jul, 2015 | Pubmed ID: 25855803 Mutations in PGAP3 Impair GPI-anchor Maturation, Causing a Subtype of Hyperphosphatasia with Mental Retardation American Journal of Human Genetics. Feb, 2014 | Pubmed ID: 24439110 Новые стратегии, сочетающей массив CGH, всего exome последовательности и в утробе матери электропорации грызунов для выявления причинных генов для пороки развития головного мозга Valerio Conti*1, Aurelie Carabalona*2,3,15, Emilie Pallesi-Pocachard2,3,4, Richard J. Leventer5,6,7, Fabienne Schaller2,3,8, Elena Parrini1, Agathe A. Deparis2,3, Françoise Watrin2,3, Emmanuelle Buhler2,3,8, Francesca Novara9, Stefano Lise10, Alistair T. Pagnamenta10, Usha Kini11, Jenny C. Taylor10, Orsetta Zuffardi9,12, Alfonso Represa2,3, David Antony Keays13, Renzo Guerrini1,14, Antonio Falace2,3, Carlos Cardoso2,3 1University of Florence, 2INSERM INMED, 3Aix-Marseille University, 4Plateforme Biologie Moléculaire et Cellulaire INMED, 5Royal Children's Hospital, 6Murdoch Children's Research Institute, 7University of Melbourne, 8Plateforme postgenomique INMED, 9University of Pavia, 10Wellcome Trust Centre for Human Genetics, 11Oxford Radcliffe NHS Trust, 12IRCCS Casimiro Mondino Foundation, 13Research Institute of Molecular Pathology, 14IRCCS Stella Maris, 15Columbia University JoVE 53570 Neurosciences
Новые стратегии, сочетающей массив CGH, всего exome последовательности и в утробе матери электропорации грызунов для выявления причинных генов для пороки развития головного мозга Valerio Conti*1, Aurelie Carabalona*2,3,15, Emilie Pallesi-Pocachard2,3,4, Richard J. Leventer5,6,7, Fabienne Schaller2,3,8, Elena Parrini1, Agathe A. Deparis2,3, Françoise Watrin2,3, Emmanuelle Buhler2,3,8, Francesca Novara9, Stefano Lise10, Alistair T. Pagnamenta10, Usha Kini11, Jenny C. Taylor10, Orsetta Zuffardi9,12, Alfonso Represa2,3, David Antony Keays13, Renzo Guerrini1,14, Antonio Falace2,3, Carlos Cardoso2,3 1University of Florence, 2INSERM INMED, 3Aix-Marseille University, 4Plateforme Biologie Moléculaire et Cellulaire INMED, 5Royal Children's Hospital, 6Murdoch Children's Research Institute, 7University of Melbourne, 8Plateforme postgenomique INMED, 9University of Pavia, 10Wellcome Trust Centre for Human Genetics, 11Oxford Radcliffe NHS Trust, 12IRCCS Casimiro Mondino Foundation, 13Research Institute of Molecular Pathology, 14IRCCS Stella Maris, 15Columbia University JoVE 53570 Neurosciences