Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ignacio Blanco-Guillermo"'
Autor:
Teresa, Pàmpols Ros, Antonio, Pérez Aytés, José Miguel, García Sagredo, Aránzazu, Díaz de Bustamante, Ignacio, Blanco Guillermo
Publikováno v:
Revista espanola de salud publica. 96
Genome sequencing is a very attractive technology as it is also the idea of sequencing children at birth, with the aim to establish medical care and preventive actions during their whole life, tailored to the genome of each newborn. Part I of this ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8b03eec1fb334241a0a87b6b0b118cf
https://pubmed.ncbi.nlm.nih.gov/35283479
https://pubmed.ncbi.nlm.nih.gov/35283479
Autor:
Teresa, Pàmpols Ros, Antonio, Pérez Aytés, José Miguel, García Sagredo, Aránzazu, Díaz de Bustamante, Ignacio, Blanco Guillermo
Publikováno v:
Revista espanola de salud publica. 96
In 2003 at the ending of the Human Genome Project, it aroused the idea that all newborns could be sequenced and its genome archived in the clinical record, in order to manage risks of diseases and response to medicaments along his whole life. Eightee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::35aba17d2f2033ac92436a2d9386e953
https://pubmed.ncbi.nlm.nih.gov/35115483
https://pubmed.ncbi.nlm.nih.gov/35115483
Autor:
Carmen Yagüe-Muñoz, Ignacio Blanco-Guillermo, Esther Cabrera-Torres, Gemma Llort-Pursals, Anna Schiaffino-Rubinat
Publikováno v:
Enfermería Clínica. 16:112-118
Resumen Objetivos Conocer el grado de conocimientos sobre el cancer, la percepcion de riesgo y el estado emocional de las personas con historia familiar de cancer de mama y cancer colorrectal que acuden a una unidad de consejo genetico (UCG). Metodo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af77c48003181e7178992234f4bf2fd0
https://doi.org/10.1016/s1130-8621(06)71197-4
https://doi.org/10.1016/s1130-8621(06)71197-4
Autor:
Gemma, Llort, Carmen Yagüe, Muñoz, Mercè Peris, Tuser, Ignacio Blanco, Guillermo, José Ramón Germà, Lluch, Allen E, Bale, Mayra Alvarez, Franco
Publikováno v:
Human Mutation. 19:307-307
BRCA1 and BRCA2 mutations underlie a substantial proportion of all hereditary breast cancer. The mutational spectrum in these genes is very broad, with hundreds of different BRCA mutations reported worldwide. However, high frequency founder mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::297dd031e94db0029bddc37c56f49984
https://doi.org/10.1002/humu.9014.abs
https://doi.org/10.1002/humu.9014.abs
Autor:
Ignacio Blanco Guillermo, Carmen Muñoz, Gemma Llort, Mayra Alvarez Franco, Allen E. Bale, José Ramón Germà Lluch, Mercè Peris Tuser
Publikováno v:
Human Mutation. 19:307-307
BRCA1 and BRCA2 mutations underlie a substantial proportion of all hereditary breast cancer. The mutational spectrum in these genes is very broad, with hundreds of different BRCA mutations reported worldwide. However, high frequency founder mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e250cadcf2b042126e1882f2a5427286
https://doi.org/10.1002/humu.9014
https://doi.org/10.1002/humu.9014