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Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis

✍ Scribed by 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

Book ID: 117852481
Publisher: American Society of Human Genetics
Year: 1998
Tongue: English
Weight: 259 KB
Volume: 63
Category: Article
ISSN: 0002-9297
DOI: 10.1086/301935

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