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Piotrowski, T., Ahn, D., Schilling, T.F., Nair, S., Ruvinsky, I., Geisler, R., Rauch, G., Haffter, P., Zon, L.I., Zhou, Y., Foott, H., Dawid, I.B. and Ho, R.K (2003) The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans. Development, 130, 5043-5052. doi:10.1242/dev.00704

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