Primary Microcephaly
Publisher
Springer New York
Reference17 articles.
1. Awad, S., Al-Dosari, M. S., Al-Yacoub, N., et al. (2013). Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis. Human Molecular Genetics, 22, 2200–2213. 2. Desir, J., Cassart, M., David, P., et al. (2008). Primary microcephaly with ASPM mutation shows simplified cortical gyration with antero-posterior gradient pre- and post-natally. American Journal of Medical Genetics. Part A, 146A, 1439–1443. 3. Genin, A., Desir, J., Lambert, N., et al. (2012). Kinetochore KMN network gene CASC5 mutated in primary microcephaly. Human Molecular Genetics, 21, 5306–5317. 4. Hussain, M. S., Baig, S. M., Neumann, S., et al. (2012). A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function. American Journal of Human Genetics, 90, 871–878. 5. Jackson, A. P., Eastwood, H., Bell, S. M., et al. (2002). Identification of microcephalin, a protein implicated in determining the size of the human brain. American Journal of Human Genetics, 71, 136–142.
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