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1دورية أكاديمية
المؤلفون: Dias, K. R., Carlston, C. M., Blok, L. E. R., De Hayr, L., Nawaz, U., Evans, C. A., Bayrak-Toydemir, P., Htun, S., Zhu, Y., Ma, A., Lynch, S. A., Moorwood, C., Stals, K., Ellard, S., Bainbridge, M. N., Friedman, J., Pappas, J. G., Rabin, R., Nowak, C. B., Douglas, J., Wilson, T. E., Guillen Sacoto, M. J., Mullegama, S. V., Palculict, T. B., Kirk, E. P., Pinner, J. R., Edwards, M., Montanari, F., Graziano, C., Pippucci, T., Dingmann, B., Glass, I., Mefford, H. C., Shimoji, T., Suzuki, T., Yamakawa, K., Streff, H., Schaaf, C. P., Slavotinek, A. M., Voineagu, I., Carey, J. C., Buckley, M. F., Schenck, A., Harvey, R. J., Roscioli, T.
مصطلحات موضوعية: Brain/metabolism, Gene Expression Regulation, Humans, Intellectual Disability/genetics, Neurodevelopmental Disorders/genetics/metabolism, Protein Domains, Whole Exome Sequencing, Developmental delay, Intellectual disability, Protein hub, Zmynd8
العلاقة: https://linkinghub.elsevier.com/retrieve/pii/S1098-3600Test(22)00803-6; Genet Med. 2022 Sep;24(9):1952-1966. doi:10.1016/j.gim.2022.06.001. Epub 2022 Aug 1.; https://rde.dspace-express.com/handle/11287/622662Test; Genetics in medicine
الإتاحة: https://doi.org/10.1016Test/j.gim.2022.06.001
https://rde.dspace-express.com/handle/11287/622662Test -
2دورية أكاديمية
المؤلفون: Goergen, S. K., Alibrahim, E., Christie, J., Dobrotwir, A., Fahey, M., Fender, L., Frawley, K., Manikkam, S. A., Pinner, J. R., Sinnott, S., Romaniello, R., Sandaradura, S. A., Taylor, J., Vasudevan, A., Righini, A.
المصدر: American Journal of Neuroradiology; Aug2021, Vol. 42 Issue 8, p1528-1534, 7p