Ventricular septal defect in Crouzon Syndrome: case report.

Hazan, F; Aykut, A; Unalp, A; Mese, T; Unal, N; Onay, H; Ozkinay, F

Hazan, F; Aykut, A; Unalp, A; Mese, T; Unal, N; Onay, H; Ozkinay, F.

Genet Couns ; 23(4): 519-22, 2012.

Article in En | MEDLINE | ID: mdl-23431754

Subject(s)

Craniofacial Dysostosis/genetics; Heart Septal Defects, Ventricular/genetics; Mutation/genetics; Receptor, Fibroblast Growth Factor, Type 2/genetics; Child; Craniofacial Dysostosis/diagnosis; Developmental Disabilities/genetics; Facies; Female; Heart Septal Defects, Ventricular/diagnosis; Humans; Intellectual Disability/genetics; Middle Aged; Turkey; Ultrasonography; Ventricular Septum/diagnostic imaging

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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

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