Identification and interruption of inheritance of familial cryptic translocations: A case report.
Mol Genet Genomic Med
; 12(1): e2356, 2024 Jan.
Article
in En
| MEDLINE
| ID: mdl-38284442
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Translocation, Genetic
/
Genetic Testing
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Mol Genet Genomic Med
Year:
2024
Document type:
Article
Affiliation country:
China
Country of publication:
Estados Unidos