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8501by Aghaei, N., Asadzadeh Aghdaei, H., Kamaliyan, Z., Mirfakhraie, R., Mohseni, R., Moshiri, A., Nazemalhosseini-Mojarad, E., Sadeghi, H., Sahebi, U., Zali, M.RSubjects: “...genotype...”
Published 2021
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8502by Lindemann, A., Myers, J.N, Osman, A.A, Patel, A.A, Takahashi, H., Takahashi, Y., Tanaka, N., Zhao, M.Subjects: “...genotype...”
Published 2018
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8503by Barros-Filho, M.C, Carvalho, A.L, Chulam, T., Drigo, S.A, Hatakeyama, M., Kowalski, L.P, Marchi, F.A, Nicolau, U.R, Pinto, C.A.L, Reis-Rosa, L.A, Rogatto, S.R, Scapulatempo-Neto, C.Subjects: “...genotype...”
Published 2018
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8504Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndromeby Alkhunaizi, E., Brandt, T., Chitayat, D.A, DeFilippo, C.P, Douglas, G.V, Dubbs, H.A, Elloumi, H.Z, Glassford, M.R, Graf, W.D, Hannibal, M.C, Héron, B., Kim, L.E, Marco, E.J, Mignot, C., Monaghan, K.G, Morrow, M.M, Myers, K.A, Parikh, S., Quinonez, S.C, Rajabi, F., Sarnat, H.B, Shankar, S.P, Shinawi, M.S, Steele, J.L, van de Kamp, J.J.P, Veerapandiyan, A., Waldman, A.TSubjects: “...genotype phenotype correlation...”
Published 2022
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Article