Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100,000 Genomes Project.
J Med Genet
; 59(8): 737-747, 2022 08.
Article
in En
| MEDLINE
| ID: mdl-34716235
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Abnormalities, Multiple
/
Eye Abnormalities
/
Kidney Diseases, Cystic
/
Ciliopathies
Type of study:
Diagnostic_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
J Med Genet
Year:
2022
Document type:
Article
Affiliation country:
Reino Unido