Prader–Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15—case report plus review of similar cases

Thomas Liehr, Elke Brude, Gabriele Gillessen-Kaesbach, Rainer König, Kristin Mrasek, Ferdinand von Eggeling, Heike Starke
  • European Journal of Medical Genetics, April 2005, Elsevier
  • DOI: 10.1016/j.ejmg.2005.01.004
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The following have contributed to this page: Professor Ferdinand von Eggeling