SNP arrays in Beckwith–Wiedemann syndrome: An improved diagnostic strategy

Author:

Keren Boris,Chantot-Bastaraud Sandra,Brioude Frédéric,Mach Corinne,Fonteneau Eric,Azzi Salah,Depienne Christel,Brice Alexis,Netchine Irène,Le Bouc Yves,Siffroi Jean-Pierre,Rossignol Sylvie

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference15 articles.

1. Macroglossia, omphalocele, adrenal cytomegaly, gigantism, and hyperplastic visceromegaly in a mother and her son;Beckwith;Birth Defects Orig. Artic. Ser.,1969

2. Das EMG-syndrome: exomphalos, Makroglossie, Gigantismus and Kholenhydratsoffwechselstoerung;Wiedemann;Z. Kinderheilkd.,1969

3. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome;Cooper;Eur. J. Hum. Genet.,2005

4. Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS);Bliek;J. Pediatr.,2004

5. Beckwith-Wiedemann syndrome;Weksberg;Am. J. Med. Genet. C Semin. Med. Genet.,2005

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