CCDC22: a novel candidate gene for syndromic X-linked intellectual disability
- Creator: 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.
- Resource Type: journal article
- Date: 2012
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
- Creator: 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.
- Resource Type: journal article
- Date: 2009