Ventricular septal defect in Crouzon Syndrome: case report.
Genet Couns
; 23(4): 519-22, 2012.
Article
in En
| MEDLINE
| ID: mdl-23431754
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Craniofacial Dysostosis
/
Receptor, Fibroblast Growth Factor, Type 2
/
Heart Septal Defects, Ventricular
/
Mutation
Type of study:
Diagnostic_studies
Limits:
Child
/
Female
/
Humans
/
Middle aged
Country/Region as subject:
Asia
Language:
En
Journal:
Genet Couns
Journal subject:
ETICA
/
GENETICA MEDICA
Year:
2012
Document type:
Article