Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation (Q34574663)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation |
scientific article |
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Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation (English)
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Matthew A Deardorff
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Maninder Kaur
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Dinah Yaeger
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Abhinav Rampuria
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Juan Pie
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Concepcion Gil-RodrÃguez
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MarÃa Arnedo
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Antonie D Kline
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Meredith Wilson
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Kaj Lillquist
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Victoria Siu
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Laird S Jackson
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Ian D Krantz
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17 January 2007
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80
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3
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485-494
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