A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus

Marcella Zollino, Giuseppe Marangi, Giovanni Neri, Daniela Orteschi, V. De Crescenzo, V. Pecile, A. Riccio

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)429-432
Number of pages4
JournalJOURNAL OF MEDICAL GENETICS
Publication statusPublished - 2010

Keywords

  • BECKWITH_WIEDEMANN
  • BWS locus
  • cryptic 11p15

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