Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.
Genet Med
; 21(4): 867-876, 2019 04.
Article
in En
| MEDLINE
| ID: mdl-30190611
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Neurofibromatosis 1
/
Neurofibroma, Plexiform
/
Neurofibromin 1
/
Learning Disabilities
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
Language:
En
Year:
2019
Type:
Article