Toward a better definition of EPCAM deletions in Lynch Syndrome: Report of new variants in Italy and the associated molecular phenotype.
Mol Genet Genomic Med
; 7(5): e587, 2019 05.
Article
in En
| MEDLINE
| ID: mdl-30916491
Full text:
1
Database:
MEDLINE
Main subject:
Colorectal Neoplasms, Hereditary Nonpolyposis
/
Gene Deletion
/
Epithelial Cell Adhesion Molecule
/
Gene Frequency
Type of study:
Risk_factors_studies
Limits:
Adult
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Year:
2019
Type:
Article