Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis
The American Journal of Human Genetics1998Vol. 63(1), pp. 170–180
Citations Over TimeTop 10% of 1998 papers
Karin Buiting, Bärbel Dittrich, Stephanie Groß, Christina Lich, Claudia Färber, Tina Buchholz, Ellie Smith, André Reis, Joachim Bürger, Markus M. Nöthen, U. Barth-Witte, Bart Janssen, Dvorah Abeliovich, Israela Lerer, Ans M.W. van den Ouweland, Dicky Halley, Connie Schrander‐Stumpel, H.J.M. Smeets, Peter Meinecke, Sue Malcolm, Anne Gardner, Marc Lalande, Robert D. Nicholls, K. Friend, Astrid Schulze, Gert Matthijs, Hannaleena Kokkonen, P Hilbert, Lionel Van Maldergem, G. Glóver, Pablo Carbonell, P J Willems, Gabriele Gillessen-Kaesbach, Bernhard Horsthemke
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