Prenatal diagnosis of craniomaxillofacial malformations: a characterization of phenotypes in trisomies 13, 18, and 21 by ultrasound and pathology.
Cleft Palate Craniofac J
; 47(2): 189-96, 2010 Mar.
Article
in En
| MEDLINE
| ID: mdl-19860526
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Trisomy
/
Ultrasonography, Prenatal
/
Chromosomes, Human, 13-15
/
Chromosomes, Human, 16-18
/
Chromosomes, Human, 21-22 and Y
/
Craniofacial Abnormalities
/
Maxillofacial Abnormalities
Type of study:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
Limits:
Adult
/
Female
/
Humans
/
Male
/
Newborn
Language:
En
Journal:
Cleft Palate Craniofac J
Journal subject:
ODONTOLOGIA
Year:
2010
Document type:
Article
Affiliation country:
Netherlands
Country of publication:
United States