Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway (Q24308083)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway |
scientific article |
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Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway (English)
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December 1996
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5
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12
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2027-32
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