Clinical Validation of a Myeloid Next-Generation Sequencing Panel for Single-Nucleotide Variants, Insertions/Deletions, and Fusion Genes.
J Mol Diagn
; 22(2): 208-219, 2020 02.
Article
in En
| MEDLINE
| ID: mdl-31751678
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Oncogene Proteins, Fusion
/
Genetic Predisposition to Disease
/
Polymorphism, Single Nucleotide
/
Myeloid Cells
/
INDEL Mutation
/
High-Throughput Nucleotide Sequencing
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
J Mol Diagn
Journal subject:
BIOLOGIA MOLECULAR
Year:
2020
Document type:
Article
Country of publication: