1. 2015
  2. Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans

    Ercan-Sencicek, A. G., Jambi, S., Franjic, D., Nishimura, S., Li, M., El-Fishawy, P., Morgan, T. M., Sanders, S. J., Bilguvar, K., Suri, M., Johnson, M. H., Gupta, A. R., Yuksel, Z., Mane, S., Grigorenko, E., Picciotto, M., Alberts, A. S., Gunel, M., Šestan, N. & State, M. W., 20 Feb 2015, In: European Journal of Human Genetics. 23, 2, p. 165-172 8 p.

    Research output: Contribution to journalArticlepeer-review

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ID: 9383843