Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1. (Q40492792)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1. |
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Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1. (English)
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Rebecca L Poole
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Donald J Leith
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Louise E Docherty
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Mansur E Shmela
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Christine Gicquel
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Miranda Splitt
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I Karen Temple
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Deborah J G Mackay
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24 August 2011
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20
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240-243
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