A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology
Talseth-Palmer, B. A., Bowden, N. A., Scott, R. J., Meldrum, C., Nicholl, J., Thompson, E., Friend, K., Liebelt, J., Bratkovic, D., Haan, E., Yu, S.
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.
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