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Prenatal diagnosis of craniomaxillofacial malformations: a characterization of phenotypes in trisomies 13, 18, and 21 by ultrasound and pathology.
Ettema, A M; Wenghoefer, M; Hansmann, M; Carels, C E L; Borstlap, W A; Bergé, S J.
Affiliation
  • Ettema AM; Department of Oral and Maxillofacial Surgery, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.
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

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