Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jurado, Luis Pérez"'
Autor:
López-López, Daniel, Roldán, Gema, Fernández-Rueda, Jose L., Bostelmann, Gerrit, Carmona, Rosario, Aquino, Virginia, Perez-Florido, Javier, Ortuño, Francisco, Pita, Guillermo, Núñez-Torres, Rocío, González-Neira, Anna, Alonso, Angel, Salgado-Garrido, Josefa, Pasalodos-Sanchez, Sara, Ayuso, Carmen, Minguez, Pablo, Avila-Fernandez, Almudena, Corton, Marta, Artuch, Rafael, Borrego, Salud, Antiñolo, Guillermo, Carracedo, Angel, Amigo, Jorge, Castaño, Luis Antonio, Tejada, Isabel, Delmiro, Aitor, Espinos, Carmina, Grinberg, Daniel, Guillén, Encarnación, Lapunzina, Pablo, Lopez-Escámez, Jose Antonio, Gallego-Martinez, Alvaro, Martí, Ramón, Rovira, Eulalia, Millán, José Mª, Moreno, Miguel Angel, Morin, Matías, Moreno-Galdó, Antonio, Fernández-Cancio, Mónica, Morte, Beatriz, Mulero, Victoriano, García, Diana, Nunes, Virginia, Palau, Francesc, Perez, Belén, Jurado, Luis Pérez, Perona, Rosario, Pujol, Aurora, Ramos, Feliciano, Lopez, Esther, Ribes, Antonia, Rosell, Jordi, Surrallés, Jordi, Peña-Chilet, María, Dopazo, Joaquin
Background Despite being a very common type of genetic variation, the distribution of copy-number variations (CNVs) in the population is still poorly understood. The knowledge of the genetic variability, especially at the level of the local populatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bb698a80a6d62488a2e50653780044e
https://hdl.handle.net/2454/45578
https://hdl.handle.net/2454/45578
Autor:
Laurie, Steven, Piscia, Davide, Matalonga, Leslie, Corvó, Alberto, Fernández-Callejo, Marcos, Garcia-Linares, Carles, Hernandez-Ferrer, Carles, Luengo, Cristina, Martínez, Inés, Papakonstantinou, Anastasios, Picó-Amador, Daniel, Protasio, Joan, Thompson, Rachel, Tonda, Raul, Bayés, Mònica, Bullich, Gemma, Camps-Puchadas, Jordi, Paramonov, Ida, Trotta, Jean-Rémi, Alonso, Angel, Attimonelli, Marcella, Béroud, Christophe, Bros-Facer, Virginie, Buske, Orion J, Cañada-Pallarés, Andrés, Fernández, José M, Hansson, Mats G, Horvath, Rita, Jacobsen, Julius O B, Kaliyaperumal, Rajaram, Lair-Préterre, Séverine, Licata, Luana, Lopes, Pedro, López-Martín, Estrella, Mascalzoni, Deborah, Monaco, Lucia, Pérez-Jurado, Luis A, Posada De la Paz, Manuel, Rambla, Jordi, Rath, Ana, Riess, Olaf, Robinson, Peter N, Salgado, David, Smedley, Damian, Spalding, Dylan, 't Hoen, Peter A C, Töpf, Ana, Zaharieva, Irina, Graessner, Holm, Gut, Ivo G, Lochmüller, Hanns, Beltran, Sergi, Corvo, Alberto, Garcia, Carles, Fernandez‐Callejo, Marcos, Hernandez, Carles, Ntalis, Anastasios Papakonstantinou, Protassio, Joan, Martinez, Ines, Pico, Daniel, Bayes, Monica, Camps, Jordi, Trotta, Jean‐Remi, Bros‐Facer, Virginie, Buske, Orion, Cañada, Andrés, Fernandez, Josè Maria, Hansson, Mats, Jacobsen, Julius, Lair, Severine, López‐Martin, Estrella, Jurado, Luis Pérez, Posada, Manuel, Robinson, Peter, Spalding, Dylan J., 't Hoen, Peter‐Bram, Gut, Ivo, Lochmúller, Hanns
Publikováno v:
Human Mutation: Variation, Informatics and Disease, 43(6), 717-733. WILEY
Academica-e. Repositorio Institucional de la Universidad Pública de Navarra
instname
Human Mutation
Academica-e. Repositorio Institucional de la Universidad Pública de Navarra
instname
Human Mutation
Rare disease patients are more likely to receive a rapid molecular diagnosis nowadays thanks to the wide adoption of next-generation sequencing. However, many cases remain undiagnosed even after exome or genome analysis, because the methods used miss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ff0fc29121e729a92e245623f303623
https://hdl.handle.net/2454/43348
https://hdl.handle.net/2454/43348
Publikováno v:
Genomics; April 1997, Vol. 41 Issue: 2 p243-249, 7p