Browsing by Author Ramos, Feliciano J.
Showing results 1 to 4 of 4
| Issue Date | Title | Author(s) |
|---|---|---|
| 1-Jul-2016 | A view on clinical genetics and genomics in Spain: of challenges and opportunities | Pàmpols i Ros, Teresa; Ramos, Feliciano J.; Lapunzina, Pablo; Gozalo Salellas, Ignasi; Pérez Jurado, Luis; Pujol Onofre, Aurora |
| 7-Jun-2012 | Cornelia de Lange syndrome with NIBPL mutation and mosaic Turner syndrome in the same individual | Wierzba, Jolanta; Gil-Rodríguez, María Concepción; Polucha, Anna; Puisac, Beatriz; Arnedo, María; Teresa-Rodrigo, María Esperanza; Winnicka, Dorota; Hegardt, Fausto; Ramos, Feliciano J.; Limon, Janusz; Pié, Juan |
| 27-Jul-2021 | Disruption of NIPBL/Scc2 in Cornelia de Lange Syndrome provokes cohesin genome-wide redistribution with an impact in the transcriptome | Garcia, Patricia; Fernández Hernández, Rita; Cuadrado, Ana; Coca, Ignacio; Gomez, Antonio; Maqueda, Maria; Latorre Pellicer, Ana; Puisac, Beatriz; Ramos, Feliciano J.; Sandoval, Juan; Esteller, Manel; Mosquera Mayo, José Luís; Rodriguez, Jairo; Pié, J.; Losada, Ana; Queralt Badia, Ethel |
| 1-Jun-2009 | Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desmin | Piñol Ripoll, Gerard; Shatunov, Alexey; Cabello, Ana; Larrode, Pilar; Puerta, Iris de la; Pelegrín, Juana; Ramos, Feliciano J.; Olivé i Plana, Montserrat; Goldfarb, Lev G. |