Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia (Q21144959)
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- Whole-Exome Re-Sequencing in a Family Quartet Identifies POP1 Mutations As the Cause of a Novel Skeletal Dysplasia
| Language | Label | Description | Also known as |
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| English | Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia |
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Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia (English)
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Matthew A Brown
Matthew A
Brown
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Gethin P Thomas
Gethin P
Thomas
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Evgeny A Glazov
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Andreas Zankl
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Marina Donskoi
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Graeme R Clark
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March 2011
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7
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e1002027
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24 March 2011
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