Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.

No abstract is available for this paper.

• Publication year

  2001

• Venue

  Annual review of genomics and human genetics (Print)

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1146/ANNUREV.GENOM.2.1.153PMID 11701647
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion.

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