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De novo point mutations in patients diagnosed with ataxic cerebral palsy by Parolin Schnekenberg, R, Perkins, EM, Miller, JW, Davies, WIL, D'Adamo, M, Pessia, M, Fawcett, KA, Sims, D, Gillard, E, Hudspith, K, Skehel, P, Williams, J, O'Regan, M, Jayawant, S, Jefferson, R, Hughes, S, Lustenberger, A, Ragoussis, J, Jackson, M, Tucker, SJ, Németh, AH
Published 2015Journal article -
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Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model. by Németh, A, Kwasniewska, A, Lise, S, Parolin Schnekenberg, R, Becker, E, Bera, K, Shanks, M, Gregory, L, Buck, D, Zameel Cader, M, Talbot, K, de Silva, R, Fletcher, N, Hastings, R, Jayawant, S, Morrison, P, Worth, P, Taylor, M, Tolmie, J, O'Regan, M, Valentine, R, Packham, E, Evans, J, Seller, A, Ragoussis, J
Published 2013Journal article