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of 4
pro vyhledávání: '"Juan L. García-Hernández"'
Autor:
Juan L. García-Hernández, Luis A. Corchete, Íñigo Marcos-Alcalde, Paulino Gómez-Puertas, Carmen Fons, Pedro A. Lazo
Publikováno v:
Human Genomics, Vol 15, Iss 1, Pp 1-11 (2021)
Abstract Background Complex developmental encephalopathy syndromes might be the consequence of unknown genetic alterations that are likely to contribute to the full neurological phenotype as a consequence of pathogenic gene combinations. Methods To i
Externí odkaz:
https://doaj.org/article/1e7d521c22ca40d9b075d128f52b3343
Autor:
Luis A. Corchete, Pedro A. Lazo, Iñigo Marcos-Alcalde, Juan L. García-Hernández, Carmen Fons, Paulino Gómez-Puertas
Publikováno v:
Human Genomics
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
instname
Digital.CSIC. Repositorio Institucional del CSIC
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Human Genomics, Vol 15, Iss 1, Pp 1-11 (2021)
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
instname
Digital.CSIC. Repositorio Institucional del CSIC
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Human Genomics, Vol 15, Iss 1, Pp 1-11 (2021)
© The Author(s).
[Background]: Complex developmental encephalopathy syndromes might be the consequence of unknown genetic alterations that are likely to contribute to the full neurological phenotype as a consequence of pathogenic gene combinati
[Background]: Complex developmental encephalopathy syndromes might be the consequence of unknown genetic alterations that are likely to contribute to the full neurological phenotype as a consequence of pathogenic gene combinati
Autor:
Francisco Vidal, Juan L. García-Hernández, Vicente Vicente, María Eugenia de la Morena-Barrio, Agustín Rodriguez-Alén, José Padilla, Noelia Rollón, Antonia Miñano, Carlos Bravo-Pérez, Nina Borràs, Belén de la Morena-Barrio, Javier Corral
Publikováno v:
British Journal of Haematology. 186
Autor:
Juan L. García-Hernández, Ricardo López-Pérez, Stela Álvarez-Fernández, Xi Chen, Atanasio Pandiella, Jesús F. San Miguel, Bruno Paiva, Elena Díaz-Rodríguez
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27583 (2011)
Digital.CSIC. Repositorio Institucional del CSIC
instname
PLoS ONE
Digital.CSIC. Repositorio Institucional del CSIC
instname
PLoS ONE
Multiple myeloma (MM) is a hematological disease characterized by an abnormal accumulation of plasma cells in the bone marrow. These cells have frequent cytogenetic abnormalities including translocations of the immunoglobulin heavy chain gene and chr