Maternal risk factors for congenital heart defects in infants with Down syndrome from Western Mexico von Corona‐Rivera, Jorge Román, Nieto‐García, Rafael, Gutiérrez‐Chávez, Andrea S., Bobadilla‐Morales, Lucina, Rios‐Flores, Izabel M., Corona‐Rivera, Alfredo, Fabián‐Morales, Gerardo E., Zavala‐Cortés, Ignacio, Lugo‐Iglesias, Cynthia, Peña‐Padilla, Christian

Volltext

Frequency of chromosome 22q11.2 deletion among newborns with non-syndromic congenital heart defects from western Mexico von Gerardo E. Fabián-Morales, Lucina Bobadilla-Morales, Christian Peña-Padilla, Rafael Nieto-García, Pascuala B. Rivera-Ramírez, Alfredo Corona-Rivera, Aurea Márquez-Mora, Graciela Macías-Salcedo, Idalid Cuero-Quezada, Jorge R. Corona-Rivera

Volltext

Identification of Pathogenic Copy Number Variants in Mexican Patients With Inherited Retinal Dystrophies Applying an Exome Sequencing Data‐Based Read‐Depth Approach von Fabian‐Morales, Gerardo E., Ordoñez‐Labastida, Vianey, Garcia‐Martínez, Froylan, Montes‐Almanza, Luis, Zenteno, Juan C.

Volltext

Frequency of chromosome 22q11.2 deletion among newborns with non-syndromic congenital heart defects from western Mexico von Fabián-Morales, Gerardo E., Bobadilla-Morales, Lucina, Peña-Padilla, Christian, Nieto-García, Rafael, Rivera-Ramírez, Pascuala B., Corona-Rivera, Alfredo, Márquez-Mora, Aurea, Macías-Salcedo, Graciela, Cuero-Quezada, Idalid, Corona-Rivera, Jorge R.

Volltext