(Q51907635)
Statements
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A novel autosomal recessive malformation syndrome associated with developmental delay and distinctive facies maps to 16ptel in the Hutterite population. (English)
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Kym M Boycott
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Chandree Beaulieu
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A Micheil Innes
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Jillian S Parboosingh
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Erik G Puffenberger
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D Ross McLeod
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1 June 2010
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152A
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6
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1349-1356
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Identifiers
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