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This page is a summary of: Prader–Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15—case report plus review of similar cases, European Journal of Medical Genetics, April 2005, Elsevier,
DOI: 10.1016/j.ejmg.2005.01.004.
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