Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis

por Rozas, M. Fernanda, Benavides, Felipe, León, Luis, Repetto, Gabriela M.
Publicado 2019

Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients

por León, Luis E., Benavides, Felipe, Espinoza, Karena, Vial, Cecilia, Alvarez, Patricia, Palomares, Mirta, Lay-Son, Guillermo, Miranda, Macarena, Repetto, Gabriela M.
Publicado 2017

Case fatality rate and associated factors in patients with 22q11 microdeletion syndrome: a retrospective cohort study

por Repetto, Gabriela M, Guzmán, M Luisa, Delgado, Iris, Loyola, Hugo, Palomares, Mirta, Lay-Son, Guillermo, Vial, Cecilia, Benavides, Felipe, Espinoza, Karena, Alvarez, Patricia
Publicado 2014

No association between genetic variants in MAOA, OXTR, and AVPR1a and cooperative strategies

por Rivera-Hechem, María I., Rodríguez-Sickert, Carlos, Guzmán, Ricardo A., Ramírez-Parada, Tadeo, Benavides, Felipe, Landaeta-Torres, Víctor, Aspé-Sánchez, Mauricio, Repetto, Gabriela M.
Publicado 2020

Intrathecal Transplantation of Autologous and Allogeneic Bone Marrow-Derived Mesenchymal Stem Cells in Dogs

por Benavides, Felipe Pérez, Pinto, Giovana Boff Araujo, Heckler, Marta Cristina Thomas, Hurtado, Diana Milena Rodríguez, Teixeira, Livia Ramos, Monobe, Marina Mitie de Souza, Machado, Gisele Fabrino, de Melo, Guilherme Dias, Rodríguez-Sánchez, Diego Noé, Alvarenga, Fernanda da Cruz Landim e, Amorim, Rogério Martins
Publicado 2021