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Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith–Magenis syndrome minimum deletion to ~650 kb

✍ Scribed by Jacqueline Schoumans; Johan Staaf; Göran Jönsson; Johanna Rantala; Kerstin Sars Zimmer; Åke Borg; Magnus Nordenskjöld; Britt-Marie Anderlid

Book ID: 116432814
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 255 KB
Volume: 48
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2005.05.004

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