Targeted next-generation sequencing for detection of PIK3CA mutations in archival tissues from patients with Klippel-Trenaunay syndrome in an Asian population : List the full names and institutional addresses for all authors.
Orphanet J Rare Dis
; 18(1): 270, 2023 09 04.
Article
in En
| MEDLINE
| ID: mdl-37667289
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Klippel-Trenaunay-Weber Syndrome
Type of study:
Diagnostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Orphanet J Rare Dis
Journal subject:
MEDICINA
Year:
2023
Document type:
Article
Affiliation country:
Country of publication: