A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short‐lived infant

por Domínguez, María Guadalupe, Rivera, Horacio, Dávalos‐Pulido, Rosa María, Dávalos‐Rodríguez, Ingrid Patricia
Publicado 2020

22q11.2 deletion detected by in situ hybridization in Mexican patients with velocardiofacial syndrome-like features

por Ramírez-Velazco, Azubel, Rivera, Horacio, Vásquez-Velázquez, Ana Isabel, Aguayo-Orozco, Thania Alejandra, Delgadillo-Pérez, Saturnino, Domínguez, Maria Guadalupe
Publicado 2018