A novel description of a syndrome consisting of 7q21.3 deletion including DYNC1I1 with preserved DLX5/6 without ectrodactyly: a case report

بواسطة Ramos-Zaldívar, Héctor M., Martínez-Irías, Daniel G., Espinoza-Moreno, Nelson A., Napky-Rajo, José S., Bueso-Aguilar, Tulio A., Reyes-Perdomo, Karla G., Montes-Gambarelli, Jimena A., Euceda, Isis M., Ponce-Barahona, Aldo F., Gámez-Fernández, Carlos A., Moncada-Arita, Wilberg A., Palomo-Bermúdez, Victoria A., Jiménez-Faraj, Julia E., Hernández-Padilla, Amanda G., Olivera, Denys A., Robertson, Kevin J., Leiva-Sanchez, Luis A., Herrera-Paz, Edwin Francisco
الحاوية / القاعدة J Med Case Rep (2016)