Central nervous system involvement in individuals with RASopathies.
Am J Med Genet C Semin Med Genet
; 190(4): 494-500, 2022 12.
Article
in En
| MEDLINE
| ID: mdl-36454176
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Heart Defects, Congenital
/
Noonan Syndrome
Limits:
Humans
Language:
En
Journal:
Am J Med Genet C Semin Med Genet
Journal subject:
GENETICA MEDICA
Year:
2022
Document type:
Article
Affiliation country:
Country of publication: