A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient. (Q43807044)
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scientific article published on 4 December 2013
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient. |
scientific article published on 4 December 2013 |
Statements
A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient (English)
K Higashimoto
K Jozaki
T Kosho
K Matsubara
T Fuke
D Yamada
H Yatsuki
T Maeda
Y Ohtsuka
K Nishioka
K Joh
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