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1.
Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material.
BMC Cancer
; 20(1): 291, 2020 Apr 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32264863
2.
Somatic mutations in MLH1 and MSH2 are a frequent cause of mismatch-repair deficiency in Lynch syndrome-like tumors.
Gastroenterology
; 146(3): 643-646.e8, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24333619
3.
Phenotypic and genotypic characterization of orthotopic human glioma models and its relevance for the study of anti-glioma therapy.
Brain Pathol
; 18(3): 423-33, 2008 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-18371177
4.
Reliable Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Tissue Using Single Molecule Tags.
J Mol Diagn
; 18(6): 851-863, 2016 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-27637301
5.
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.
Nat Genet
; 41(1): 112-7, 2009 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-19098912
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