Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).

No abstract is available for this paper.

• Publication year

  2004

• Venue

  Annales de Genetique

• Publication date

  2004-07-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/J.ANNGEN.2004.01.003PMID 15337472
• 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.

• Molecular characterization of a unique de novo 15q deletion associated with Prader–Willi syndrome and central visual impairment

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• Impact of molecular mechanisms, including deletion size, on Prader–Willi syndrome phenotype: study of 75 patients

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