Navegar por término MeSH "DNA Mutational Analysis"

Mostrando ítems 1-6 de 6

Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents

2015- Bodo, S.; Colas, C.; Buhard, O.; Collura, A.; Tinat, J.; [et al.]
Fast and efficient microfluidic cell filter for isolation of circulating tumor cells from unprocessed whole blood of colorectal cancer patients

2019- Ribeiro-Samy, S.; Oliveira, M. I.; Pereira Veiga, Thais; Muinelo Romay , Laura; Carvalho, S.; [et al.]
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

2015- Legati, A.; Giovannini, D.; Nicolas, G.; López-Sánchez, U.; Quintans Castro, Beatriz; [et al.]
Novel Mutation Hotspots within Non-Coding Regulatory Regions of the Chronic Lymphocytic Leukemia Genome

2020- MOSQUERA ORGUEIRA, ADRIAN; Antelo Rodríguez, Beatriz; Díaz Arias, José; Díaz Varela, Nicolás; Alonso Vence, Natalia; [et al.]
Severe Autoinflammatory Manifestations and Antibody Deficiency Due to Novel Hypermorphic PLCG2 Mutations

2020- Martín-Nalda, A.; Fortuny, C.; Rey Cordo, Carmen Lourdes; Bunney, T. D.; Alsina, L.; [et al.]
Ultra-selection of metastatic colorectal cancer patients using next-generation sequencing to improve clinical efficacy of anti-EGFR therapy

2019- J., Vidal; B., Bellosillo; C., Santos Vivas; P., Garcia-Alfonso; A., Carrato; [et al.]