Adelaide Research & Scholarship
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https://hdl.handle.net/2440/6917
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| Type: | Journal article |
| Title: | Sporadic imprinting defects in Prader-Willi-Syndrome and Angelman-Syndrome - implications for imprint-switch models, genetic counseling, and prenatal diagnosis |
| Author: | Buiting, Karin Dittrich, Barbel Gross, Stephanie Lich, Christina Farber, Claudia Buchholz, Tina Smith, Ellie Reis, Andre Burger, Joachim Nothen, Markus M. Barth-Witte, Ulli Janssen, Bart Abeliovich, Dvorah Lerer, Israela Van den Ouweland, Ans M. W. Halley, Dicky J. J. Schrander-Stumpel, Connie Smeets, Hubert Meinecke, Peter Malcolm, Susan Gardner, Anne Lalande, Marc Nicholls, Robert D. Friend, Kathryn L. Schulze, Astrid Matthjis, Gert Kokkonen, Hannaleena Hilbert, Pascale Van Maldergem, Lionel Glover, Guillermo Carbonell, Pablo Willems, Patrick Gillessen-Kaesbach, Gabriele Horsthemke, Bernhard |
| Citation: | American Journal of Human Genetics, 1998; 63(1):170-180 |
| Issue Date: | 1998 |
| ISSN: | 0002-9297 |
| Statement of Responsibility: | Karin Buiting, Bärbel Dittrich, Stephanie Groß, Christina Lich, Claudia Färber, Tina Buchholz, Ellie Smith, André Reis, Joachim Bürger, Markus M. Nöthen, Ulli Barth-Witte, Bart Janssen, Dvorah Abeliovich, Israela Lerer, Ans M.W. van den Ouweland, Dicky J.J. Halley, Connie Schrander-Stumpel, Hubert Smeets, Peter Meinecke, Sue Malcolm, Anne Gardner, Marc Lalande, Robert D. Nicholls, Kathie Friend, Astrid Schulze, Gert Matthijs, Hannaleena Kokkonen, Pascale Hilbert, Lionel Van Maldergem, Guillermo Glover, Pablo Carbonell, Patrick Willems, Gabriele Gillessen-Kaesbach, Bernhard Horsthemke |
| DOI: | 10.1086/301935 |
| Appears in Collections: | Paediatrics publications |
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