Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome.
Am J Med Genet A
; 179(9): 1783-1790, 2019 09.
Article
in En
| MEDLINE
| ID: mdl-31294511
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Brain
/
Constriction, Pathologic
/
Hepatocyte Nuclear Factor 3-beta
/
Hypopituitarism
Limits:
Humans
/
Newborn
Language:
En
Journal:
Am J Med Genet A
Journal subject:
GENETICA MEDICA
Year:
2019
Document type:
Article
Country of publication:
Estados Unidos