Beckwith-Wiedemann Syndrome

The Beckwith-Wiedemann syndrome (BWS) is a complex congenital disorder with omphalocele, macroglossia, and gigantism as its most common neonatal features. However, in individual cases, the phenotypic expression of this condition is variable. Antenatal diagnosis in previously unsuspected cases depend...

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Veröffentlicht in:The journal of maternal-fetal & neonatal medicine 1992, Vol.1 (2), p.70-74
Hauptverfasser: O'grady, John P., Tunney, Carol, Pflueger, Solveig M.V., Kanaan, Camille M., Bayer-Zwirello, Lucy, Gimovsky, Martin L., Carbone, Thomas
Format: Artikel
Sprache:eng
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