Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: Implications for imprint-switch models, genetic counseling, and prenatal diagnosis

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Persistent URL	doi.org/10.1086/301935, hdl.handle.net/1765/57733
Journal	American Journal of Human Genetics
Organisation	Department of Clinical Genetics
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Buiting, K., Dittrich, B., Groß, S., Lich, C., Färber, C., Buchholz, T., Smith, E., Reis, A., Bürger, F., Nöthen, M., Barth-Witte, U., Janssen, B., Abeliovicz, D., Lerer, B., van den Ouweland, A., Halley, D., Schrander-Stumpel, C., Smeets, H., Meinecke, P., … Horsthemke, B. (1998). Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: Implications for imprint-switch models, genetic counseling, and prenatal diagnosis. American Journal of Human Genetics, 63(1), 170–180.https://doi.org/10.1086/301935

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