(Q51946913)
Statements
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A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD. (English)
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Kym M Boycott
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Malcolm I Parslow
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Judith L Ross
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Ivan P Miller
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N Torben Bech-Hansen
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Patrick M MacLeod
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1 October 2003
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122A
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2
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139-147
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Identifiers
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