Identification through exome sequencing of the first PMM2-CDG individual of Mexican mestizo origin

por González-Domínguez, C.A., Raya-Trigueros, A., Manrique-Hernández, S., González Jaimes, A., Salinas-Marín, R., Molina-Garay, C., Carrillo-Sánchez, K., Flores-Lagunes, L.L., Jiménez-Olivares, M., Dehesa-Caballero, C., Alaez-Versón, C., Martínez-Duncker, I.
Publicado 2020

Expression levels of seven candidate genes in human peripheral blood mononuclear cells and their association with preeclampsia

por Martinez-Fierro, M. L., Garza-Veloz, I., Carrillo-Sanchez, K., Martinez-Gaytan, V., Cortes-Flores, R., Ochoa-Torres, M. A., Guerrero, G. G., Rodriguez-Sanchez, I. P., Cancela-Murrieta, C. O., Zamudio-Osuna, M., Badillo-Almaraz, J. I., Castruita-De la Rosa, C.
Publicado 2014

Non-functional alternative splicing caused by a Latino pathogenic variant in a case of PMM2-CDG

por González-Domínguez, C.A., Villarroel, C.E., Rodríguez-Morales, M., Manrique-Hernández, S., González-Jaimes, A., Olvera-Rodriguez, F., Beutelspacher, K., Molina-Garay, C., Carrillo-Sánchez, K., Flores-Lagunes, L.L., Jiménez-Olivares, M., Muñoz-Rivas, A., Cruz-Muñoz, M.E., Mora-Montes, H.M., Salinas-Marín, R., Alaez-Verson, C., Martínez-Duncker, I.
Publicado 2021