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CCDC22: a novel candidate gene for syndromic X-linked intellectual disability
- Voineagu, I., Huang, L., Field, M., Gecz, J., Geschwind, D., Winden, K., Lazaro, M., Haan, E., Nelson, J., McGaughran, J., Nguyen, L. S., Friend, K., Hackett, A.
n of 1 trial for an ornithine transcarbamylase deficiency carrier
- Hackett, A., Gillard, J., Wilcken, B.
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