Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome

por Farrera, Arodi, Villanueva, María, Vizcaíno, Alfredo, Medina-Bravo, Patricia, Balderrábano-Saucedo, Norma, Rives, Mariana, Cruz, David, Hernández-Carbajal, Elizabeth, Granados-Riveron, Javier, Sánchez-Urbina, Rocío
Publicado 2019

Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage disease

por Hu, Dan, Hu, Dong, Liu, Liwen, Barr, Daniel, Liu, Yang, Balderrabano-Saucedo, Norma, Wang, Bo, Zhu, Feng, Xue, Yumei, Wu, Shulin, Song, BaoLiang, McManus, Heather, Murphy, Katherine, Loes, Katherine, Adler, Arnon, Monserrat, Lorenzo, Antzelevitch, Charles, Gollob, Michael H., Elliott, Perry M., Barajas-Martinez, Hector
Publicado 2020