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Genetic analyses of aplastic anemia and idiopathic pulmonar..:
Arias-Salgado, Elena G
;
Galvez, Eva
;
Planas-Cerezales, Lurdes
...
Orphanet Journal of Rare Diseases;14(1). , 2019
Link:
https://hdl.handle.net/11351/4147
RT Journal T1
Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes
UL https://suche.suub.uni-bremen.de/peid=base-ftscientia:oai:scientiasalut.gencat.cat:11351_4147&Exemplar=1&LAN=DE A1 Arias-Salgado, Elena G A1 Galvez, Eva A1 Planas-Cerezales, Lurdes A1 Pintado-Berninches, Laura A1 Vallespin, Elena A1 Martinez, Pilar A1 Martín Nalda, Andrea A1 Díaz de Heredia Rubio, Maria Cristina A1 Martínez Gallo, Mónica A1 Uria Oficialdegui, Maria Luz PB BMC YR 2019 K1 Anèmia aplàstica - Aspectes genètics K1 Fibrosi pulmonar - Aspectes genètics K1 Telòmer K1 ANATOMY::Cells::Cellular Structures::Intracellular Space::Cell Nucleus::Cell Nucleus Structures::Intranuclear Space::Chromosomes::Chromosome Structures::Telomere K1 Other subheadings::Other subheadings::Other subheadings::/pathology K1 DISEASES::Hemic and Lymphatic Diseases::Hematologic Diseases::Anemia::Anemia K1 Aplastic K1 DISEASES::Respiratory Tract Diseases::Lung Diseases::Lung Diseases K1 Interstitial::Idiopathic Interstitial Pneumonias::Idiopathic Pulmonary Fibrosis K1 Other subheadings::Other subheadings::Other subheadings::/genetics K1 ANATOMÍA::células::estructuras celulares::espacio intracelular::núcleo celular::estructuras del núcleo celular::espacio intranuclear::cromosomas::estructuras cromosómicas::telómero K1 Otros calificadores::Otros calificadores::Otros calificadores::/patología K1 ENFERMEDADES::enfermedades hematológicas y linfáticas::enfermedades hematológicas::anemia::anemia aplásica K1 ENFERMEDADES::enfermedades respiratorias::enfermedades pulmonares::enfermedades pulmonares intersticiales::neumonías intersticiales idiopáticas::fibrosis pulmonar idiopática K1 Otros calificadores::Otros calificadores::Otros calificadores::/genética JF Orphanet Journal of Rare Diseases;14(1) LK http://dx.doi.org/https://hdl.handle.net/11351/4147 DO https://hdl.handle.net/11351/4147 SF ELIB - SuUB Bremen
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