Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders.
Am J Hum Genet
; 110(8): 1343-1355, 2023 08 03.
Article
in En
| MEDLINE
| ID: mdl-37541188
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genome, Human
/
Neurodevelopmental Disorders
Limits:
Humans
Language:
En
Journal:
Am J Hum Genet
Year:
2023
Document type:
Article
Country of publication: