Novel fetal and maternal sonographic findings in confirmed cases of Beckwith-Wiedemann syndrome

Author:

Kagan Karl Oliver1,Berg Christoph23,Dufke Andreas4,Geipel Annegret2,Hoopmann Markus1,Abele Harald1

Affiliation:

1. Department of Obstetrics and Gynaecology; University of Tübingen; Tübingen Germany

2. Department of Obstetrics and Gynaecology; University of Bonn; Bonn Germany

3. Department of Obstetrics and Gynaecology; University of Cologne; Cologne Germany

4. Institute of Medical Genetics and Applied Genomics; University of Tübingen; Tübingen Germany

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference28 articles.

1. Familial malformation complex with umbilical hernia and macroglossia-a “new syndrome?”;Wiedemann;J Genet Hum,1964

2. Beckwith JB Extreme cytomegaly of the adrenal fetal cortex, hyperplasia of the kidneys and pancreas, and Leydig-cell hyperplasia: another syndrome? 1963

3. Beckwith-Wiedemann syndrome;Elliott;J Med Genet,1994

4. Beckwith-Wiedemann syndrome;Weksberg;Am J Med Genet,2005

5. The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: two new reports;Wilson;Am J Med Genet,2008

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