Contribution of de novo and inherited rare CNVs to very preterm birth.
J Med Genet
; 57(8): 552-557, 2020 08.
Article
in En
| MEDLINE
| ID: mdl-32051258
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genetic Predisposition to Disease
/
Premature Birth
/
Genome-Wide Association Study
/
DNA Copy Number Variations
Type of study:
Guideline
/
Prognostic_studies
Limits:
Female
/
Humans
/
Male
/
Newborn
/
Pregnancy
Language:
En
Journal:
J Med Genet
Year:
2020
Document type:
Article
Affiliation country:
Reino Unido