Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.
Orphanet J Rare Dis
; 16(1): 6, 2021 01 06.
Article
in En
| MEDLINE
| ID: mdl-33407644
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Autism Spectrum Disorder
Type of study:
Prognostic_studies
Limits:
Female
/
Humans
/
Pregnancy
Language:
En
Journal:
Orphanet J Rare Dis
Journal subject:
MEDICINA
Year:
2021
Document type:
Article
Affiliation country:
Country of publication: