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Navegar por autor "Barros Angueira, Francisco"

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      16p11.2 microdeletion associated to early onset benign childhood seizures 

      2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Perez Gay, Laura; Dacruz Álvarez, David [et al.]
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      A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features 

      2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Castro Gago, Manuel; Eiris Puñal, Jesús; Lago Lestón, Ramón Manuel [et al.]
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      A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease 

      2014- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Couce Pico, María Luz; Balboa Beltran, Emilia; Pérez Muñuzuri, Alejandro; [et al.]
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      A pharmacogenetics study of TPMT and ITPA genes detects a relationship with side effects and clinical response in patients with inflammatory bowel disease receiving azathioprine 

      2011- Echarri Piudo, Ana; Castro Alvariño, Javier; Barreiro de Acosta, Manuel; Carracedo Álvarez, Ángel; Barros Angueira, Francisco; [et al.]
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      Activity of beta2-adrenergic receptor in oral squamous cell carcinoma is mediated by overexpression of the ADRBK2 gene: A pilot study 

      2012- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel
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      BCL10 expression is not related to any clinicopathological parameter or prognosis for oral squamous cell carcinomas in Spain 

      2012- Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; Gándara Rey, José Manuel [et al.]
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      BCL10 expression is unrelated to clinico-pathological parameters or prognoses for oral squamous cell carcinomas 

      2012- Barros Angueira, Francisco; Gayoso Diz, Pilar; Suárez Peñaranda, Jose Manuel
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      Candidate genes for azathioprine's efficacy or toxicity in inflammatory bowel disease patients using a exome-wide genotyping analysis 

      2011- Echarri Piudo, Ana; Castro Alvariño, Javier; Barreiro de Acosta, Manuel; Carracedo Álvarez, Ángel; Barros Angueira, Francisco; [et al.]
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      Current trends in miRNAs and their relationship with oral squamous cell carcinoma 

      2012- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel [et al.]
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      Delimiting allelic imbalance of TYMS by allele-specific analysis 

      2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Balboa Beltran, Emilia; Cruz Guerrero, Raquel
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      Exome-wide pharmacogenomic analysis of response to thiopurines in inflammatory bowel disease patients 

      2015- Echarri Piudo, Ana; Barreiro de Acosta, Manuel; Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Zabala Fernández, William [et al.]
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      Expression of CA IX in dysplasia adjacent to surgical resection margins of oral squamous cell carcinoma 

      2014- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]
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      Expression of CA-IX is associated with advanced stage tumors and poor survival in oral squamous cell carcinoma patients 

      2012- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]
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      Genetic study of osteogenesis imperfecta: Two novel mutations in COL1A1 and COL1A2 

      2014- Leis Trabazo, María Rosaura; Barros Angueira, Francisco; Loidi Fernández, Lourdes; Pombo Arias, Manuel; Cabanas Rodríguez, Paloma; [et al.]
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      Hypoxia-inducible factors in OSCC 

      2011- Pérez Sayáns, Mario; Barros Angueira, Francisco; Gayoso Diz, Pilar; García García, Abel; Suárez Peñaranda, Jose Manuel; [et al.]
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      Interstitial Microdeletions Including the Chromosome Band 4q13.2 and the UBA6 Gene as Possible Causes of Intellectual Disability and Behavior Disorder 

      2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Fernández Prieto, Montserrat; Castro Gago, Manuel; Gómez Lado, María del Carmen; [et al.]
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      Microdeleción 16p11.2 asociada a convulsiones benignas de la primera infancia 

      2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Perez Gay, Laura; Dacruz Álvarez, David [et al.]
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      Microdeleción 2q23.1 y hallazgos sindrómicos 

      2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Eiris Puñal, Jesús; Dacruz Álvarez, David; [et al.]
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      Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes 

      2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Castro Gago, Manuel; Perez Gay, Laura; Eiris Puñal, Jesús; [et al.]
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      Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing. 

      2011- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Barros Angueira, Francisco; Campos Balea, Begoña; Quintans Castro, Beatriz; [et al.]
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