Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE (Q34002178)
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English | Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE |
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Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE (English)
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Edwin H Cook
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Pawel Stankiewicz
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Aleksandar Milosavljevic
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Patricia B S Celestino-Soper
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Jian Li
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Michael T Murtha
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A Gulhan Ercan-Sencicek
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Lea Davis
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Susanne Thomson
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A Craig Chinault
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Zhishuo Ou
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Jennifer R German
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Matthew W State
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Arthur L Beaudet
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24 August 2011
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22
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4360-4370
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