An 11p15 Imprinting Centre Region 2 Deletion in a Family with Beckwith Wiedemann Syndrome Provides Insights into Imprinting Control at CDKN1C

Open Access

Peer-reviewed

Research Article

Elizabeth Algar ,

* E-mail: elizabeth.algar@rch.org.au

Affiliations Molecular Oncology Laboratory, Murdoch Children's Research Institute, Melbourne, Australia, Department of Paediatrics, University of Melbourne, Melbourne, Australia
⨯
Vinod Dagar,

Affiliation Molecular Oncology Laboratory, Murdoch Children's Research Institute, Melbourne, Australia
⨯
Menka Sebaj,

Affiliation Molecular Oncology Laboratory, Murdoch Children's Research Institute, Melbourne, Australia
⨯
Nicholas Pachter

Affiliation Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, Australia
⨯

Reader Comments (0)

Methylation
Is the Subject Area "Methylation" applicable to this article?

Thanks for your feedback.
DNA methylation
Is the Subject Area "DNA methylation" applicable to this article?

Thanks for your feedback.
Chromosomal deletions
Is the Subject Area "Chromosomal deletions" applicable to this article?

Thanks for your feedback.
Genetic loci
Is the Subject Area "Genetic loci" applicable to this article?

Thanks for your feedback.
Blood
Is the Subject Area "Blood" applicable to this article?

Thanks for your feedback.
Chromatin
Is the Subject Area "Chromatin" applicable to this article?

Thanks for your feedback.
Insulators
Is the Subject Area "Insulators" applicable to this article?

Thanks for your feedback.
Enhancer elements
Is the Subject Area "Enhancer elements" applicable to this article?

Thanks for your feedback.