المؤلفون: González-Acosta, Maribel, Marín, Fátima, Puliafito, Benjamin, Bonifaci, Nuria, Fernández, Anna, Navarro, Matilde, Salvador, Hector, Balaguer, Francesc, Iglesias, Silvia, Velasco, Angela, Grau Garces, Elia, Moreno, Victor, Gonzalez-Granado, Luis Ignacio, Guerra-García, Pilar, Ayala, Rosa, Florkin, Benoit, Kratz, Christian, Ripperger, Tim, Rosenbaum, Thorsten, Januszkiewicz-Lewandowska, Danuta, Azizi, Amedeo A., Ragab, Iman, Nathrath, Michaela, Pander, Hans-Jürgen, Lobitz, Stephan, Suerink, Manon, Dahan, Karin, Imschweiler, Thomas, Demirsoy, Ugur, Brunet, Joan, Lázaro, Conxi, Rueda, Daniel, Wimmer, Katharina, Capellá, Gabriel, Pineda, Marta

المصدر: Journal of Medical Genetics, 57 (4), 269-273 (2020)

مصطلحات موضوعية: Adolescent, Adult, Brain Neoplasms/blood/genetics/pathology, Child, Child, Preschool, Colorectal Neoplasms/blood/genetics/pathology, Colorectal Neoplasms, Hereditary Nonpolyposis/blood/genetics/pathology, DNA Mismatch Repair/genetics, DNA-Binding Proteins/genetics, Female, Germ-Line Mutation/genetics, Heterozygote, High-Throughput Nucleotide Sequencing, Humans, Infant, Male, Microsatellite Instability, MutS Homolog 2 Protein/genetics, Neoplastic Syndromes, Hereditary/blood/genetics/pathology, Young Adult, constitutional mismatch repair deficiency, highly sensitive methodologies, lynch syndrome, next generation sequencing, Life sciences, Genetics & genetic processes, Sciences du vivant, Génétique & processus génétiques

Relation: urn:issn:0022-2593; urn:issn:1468-6244

URL الوصول: https://orbi.uliege.be/handle/2268/266477