A multi-laboratory assessment of clinical exome sequencing for detection of hereditary disease variants: 4441 ClinVar variants for clinical genomic test development and validation.
Clin Chim Acta
; 535: 99-107, 2022 Oct 01.
Article
in En
| MEDLINE
| ID: mdl-35985503
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Diagnostic_studies
/
Guideline
/
Prognostic_studies
Language:
En
Journal:
Clin Chim Acta
Year:
2022
Document type:
Article
Country of publication:
Países Bajos