Results for POU3F2 (also called BRN2 or N-OCT3 or OCT7)

Publications & Outputs

1. Small 6q16.1 deletions encompassing POU3F2 cause susceptibility to obesity and variable developmental delay with intellectual disability

   Kasher, P. R., Shertz, K. E., Thomas, M., Jackson, A., Annunziata, S., Ballesta-Martinez, M. J., Campeau, P. M., Clayton, P. E., Eaton, J. L., Granata, T., Guille-Navarro, E., Hernando, C., Laverriere, C. E., Lieden, A., Villa-Marcos, O., McEntagart, M., Nordgren, A., Pantaleonie, C., Prebel-Richard, C., Sarret, C., & 5 othersSciacca, F. L., Wright, R., Kerr, B., Glasgow, E. & Banka, S., 4/02/2016, In: American Journal of Human Genetics. 98, 2, p. 363-372 10 p.

   Research output: Contribution to Journal/Magazine › Journal article › peer-review