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GM Mirzaa

First name:
GM
Last name:
Mirzaa
Ruggeri, G., Timms, A., Cheng, C., Weiss, A., Kollros, P., Chapman, T., … Mirzaa, G. (2018). Bi-allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus. American Journal of Medical Genetics. Part A. https://doi.org/10.1002/ajmg.a.38592 (Original work published 2018)
Fry, A., Fawcett, K., Zelnik, N., Yuan, H., Thompson, B., Shemer-Meiri, L., … Pilz, D. (2018). De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain : A Journal of Neurology. https://doi.org/10.1093/brain/awx358 (Original work published 2018)
Taylor, C., Smith, R., Lehman, C., Mitchel, M., Singer, K., Weaver, W., … Amemiya, A. 16p11.2 Recurrent Deletion. (Original work published 1993)