SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing.
Hum Genet
; 142(2): 201-216, 2023 Feb.
Article
in En
| MEDLINE
| ID: mdl-36376761
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
DNA Copy Number Variations
/
Autism Spectrum Disorder
Type of study:
Guideline
/
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Hum Genet
Year:
2023
Type:
Article
Affiliation country:
Canada