(Q46716515)
Statements
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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 approximately 650 kb. (English)
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Jacqueline Schoumans
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Johan Staaf
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Göran Jönsson
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Johanna Rantala
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Kerstin Sars Zimmer
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Ake Borg
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Britt-Marie Anderlid
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1 July 2005
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48
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3
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290-300
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