All-in-one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence-of-heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1-year experience.
Prenat Diagn
; 43(4): 527-543, 2023 04.
Article
in En
| MEDLINE
| ID: mdl-36647814
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
DNA Copy Number Variations
/
Fetus
Limits:
Female
/
Humans
/
Pregnancy
Language:
En
Journal:
Prenat Diagn
Year:
2023
Document type:
Article