Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction

• Benedetta Izzi,

  Affiliation Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium

  ⨯
• Inge Francois,

  Affiliation Departement of Pediatrics, University of Leuven, Leuven, Belgium

  ⨯
• Veerle Labarque,

  Affiliation Departement of Pediatrics, University of Leuven, Leuven, Belgium

  ⨯
• Chantal Thys,

  Affiliation Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium

  ⨯
• Christine Wittevrongel,

  Affiliation Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium

  ⨯
• Koen Devriendt,

  Affiliation Center for Human Genetics, University of Leuven, Leuven, Belgium

  ⨯
• Eric Legius,

  Affiliation Center for Human Genetics, University of Leuven, Leuven, Belgium

  ⨯
• Annick Van den Bruel,

  Affiliation General Hospital Sint Jan Brugge, Brugge, Belgium

  ⨯
• Marc D'Hooghe,

  Affiliation General Hospital Sint Jan Brugge, Brugge, Belgium

  ⨯
• Diether Lambrechts,

  Affiliation Vesalius Research Center, University of Leuven and VIB, Leuven, Belgium

  ⨯
• Francis de Zegher,

  Affiliation Departement of Pediatrics, University of Leuven, Leuven, Belgium

  ⨯
• Chris Van Geet,

  Affiliations Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium, Departement of Pediatrics, University of Leuven, Leuven, Belgium

  ⨯
• Kathleen Freson

  * E-mail: kathleen.freson@med.kuleuven.be

  Affiliation Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium

  ⨯