المؤلفون: Langhammer, F, Maroofian, R, Badar, R, Gregor, A, Rochman, M, Ratliff, JB, Koopmans, M, Herget, T, Hempel, M, Kortüm, F, Heron, D, Mignot, C, Keren, B, Brooks, S, Botti, C, Ben-Zeev, B, Argilli, E, Sherr, EH, Gowda, VK, Srinivasan, VM, Bakhtiari, S, Kruer, MC, Salih, MA, Kuechler, A, Muller, EA, Blocker, K, Kuismin, O, Park, KL, Kochhar, A, Brown, K, Ramanathan, S, Clark, RD, Elgizouli, M, Melikishvili, G, Tabatadze, N, Stark, Z, Mirzaa, GM, Ong, J, Grasshoff, U, Bevot, A, von Wintzingerode, L, Jamra, RA, Hennig, Y, Goldenberg, P, Al Alam, C, Charif, M, Boulouiz, R, Bellaoui, M, Amrani, R, Al Mutairi, F, Tamim, AM, Abdulwahab, F, Alkuraya, FS, Khouj, EM, Alvi, JR, Sultan, T, Hashemi, N, Karimiani, EG, Ashrafzadeh, F, Imannezhad, S, Efthymiou, S, Houlden, H, Sticht, H, Zweier, C

المصدر: Genetics in Medicine , 25 (8) , Article 100885. (2023)

مصطلحات موضوعية: Developmental and epileptic encephalopathy, Intellectual disability, Neurodevelopmental disorder, RHOBTB2, Seizures

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10173027/1/RHOBTB_manuscript_230331_without%20trackchanges.docx.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10173027Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10173027/1/RHOBTB_manuscript_230331_without%20trackchanges.docx.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10173027Test/

المؤلفون: Barshop, BA, Alanay, Y, Danda, S, Baek, ST, Al-Sanaa, N, Megahed, H, Al-Abdulwahed, HY, Musaev, D, Kariminejad, A, Dobyns, WB, Kaymakçalan, H, Bilguvar, K, Jamra, RA, Gunel, M, Schaffer, AE, Gleeson, JG, Breuss, MW, Scott, EC, Kayserili, H, Mojahedi, F, Chelly, J, Kara, M, Cai, N, Silhavy, JL, Kara, BÜLENT, Elsharif, S, Sukhudyan, B, Yılmaz, C, Zaki, MS, Kalur, A, Ben-Omran, T, Nachnani, R, James, KN, Rosti, RO, Caglayan, AO, Incecik, F, Stanley, V, Wang, R, Copeland, B, Fenercioglu, E, Miller, I, Mansour, L, Melikishvili, G, Faqeih, E

العلاقة: f028095c-14a8-4e94-affe-c7afb69af407; https://avesis.kocaeli.edu.tr/publication/details/f028095c-14a8-4e94-affe-c7afb69af407/oaiTest

الإتاحة: https://doi.org/10.1038/s41588-018-0166-0Test
https://avesis.kocaeli.edu.tr/publication/details/f028095c-14a8-4e94-affe-c7afb69af407/oaiTest

العنوان البديل: РАСШИРЕННЫЙ ФЕНОТИП МУТАЦИИ TMEM67 ГЕНА: ОПИСАНИЕ СЛУЧАЯ (Russian)

المؤلفون: Tkemaladze, T., Melikishvili, G., Kherkheulidze, V., Melikishvili, A., Davitaia, T.

المصدر: Georgian Medical News; Jun2017, Vol. 267 Issue 6, p100-103, 4p

المؤلفون: Melikishvili, G. A.

المصدر: Anthropology & Archeology of Eurasia; Jul1978, Vol. 17 Issue 1, p25-72, 48p

المؤلفون: Melikishvili, G. A.

المصدر: Anthropology & Archeology of Eurasia; Oct1976, Vol. 15 Issue 2/3, p29-49, 21p

المؤلفون: Melikishvili, G. A.

المصدر: Soviet Anthropology and Archeology ; volume 15, issue 2-3, page 29-49 ; ISSN 0038-528X

الإتاحة: https://doi.org/10.2753/aae1061-195915020329Test