Small mosaic deletion encompassing the snoRNAs and SNURF‐SNRPN results in an atypical Prader–Willi syndrome phenotype

No abstract is available for this paper.

• Publication year

  2014

• Venue

  American Journal of Medical Genetics. Part A

• Publication date

  2014-02-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/ajmg.a.36307PMID 24311433
• 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.

• Unique and atypical deletions in Prader–Willi syndrome reveal distinct phenotypes

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