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Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction
Authors:Izzi Benedetta  Francois Inge  Labarque Veerle  Thys Chantal  Wittevrongel Christine  Devriendt Koen  Legius Eric  Van den Bruel Annick  D'Hooghe Marc  Lambrechts Diether  de Zegher Francis  Van Geet Chris  Freson Kathleen
Affiliation:Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.
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