Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Wilkinson, R"'
Autor:
Woodgate, S. L.1 (AUTHOR), Wilkinson, R. G.2 (AUTHOR) rgwilkinson@harper-adams.ac.uk
Publikováno v:
Annals of Applied Biology. May2021, Vol. 178 Issue 3, p430-441. 12p.
Autor:
Armstrong, B., Wilkinson, R.
Publikováno v:
ISBT Science Series. 2020 Supplement, Vol. 15, p112-122. 11p.
Autor:
Morgan, Michael J.1,2 (AUTHOR) mjm18j@fsu.edu, Wilkinson, R. Tyler1 (AUTHOR), Osborn, Debra S.3 (AUTHOR)
Publikováno v:
Journal of Employment Counseling. Jun2020, Vol. 57 Issue 2, p85-96. 12p.
Autor:
Tsai, C.‐H., Abdrakhmatov, K., Mukambayev, A., Elliott, A. J., Elliott, J. R., Grützner, C., Rhodes, E. J., Ivester, A. H., Walker, R. T., Wilkinson, R.
Publikováno v:
Tectonics; Oct2022, Vol. 41 Issue 10, p1-33, 33p
Autor:
Pitman, J. P.1, Wilkinson, R.2, Basavaraju, S. V.1, Finckenstein, B.2, Smit Sibinga, C.3, Marfin, A. A.1, Postma, M. J.4,5, Mataranyika, M.6, Tobias, J.1, Lowrance, D. W.1
Publikováno v:
ISBT Science Series. Nov2014, Vol. 9 Issue 2, p325-333. 9p.
Autor:
Lawn, S. D.1,2 stevelawn@yahoo.co.uk, Wilkinson, R. J.3,4
Publikováno v:
Parasite Immunology. Nov2006, Vol. 28 Issue 11, p625-633. 9p. 1 Chart.
Autor:
Sigsworth, E. M.1, Wilkinson, R. K.2
Publikováno v:
Bulletin of Economic Research. Nov71, Vol. 23 Issue 2, p113. 16p. 15 Charts.
Akademický článek
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Autor:
Andermann, E, Jansen, Anna, Sancak, Ozgur, D'agostino, Md, Badhwar, Amanpreet, Roberts, P., Wilkinson, R., Melanson, Denis, Tampieri, Donatella, Maat-Kievit, Anneke, Goedbloed, Myriam, Van Den Ouweland, A.m., Nellist, Mark, Pandolfo, M., Sims, K., Thiele, Elizabeth, Dubeau, François, Andermann, Frederick, Kwiatkowski, David, Halley, D.
Purpose: Tuberous sclerosis complex is an autosomal dominant disorder characterised by hamartomatous growth in various organs, and caused by mutations in the TSC1 (9q34) or TSC2 (16p13) genes. Overall, TSC2 mutations have been associated with a more
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::188d24b2a085aa15d0a7bbf76b7ea43d
https://biblio.vub.ac.be/vubir/mild-phenotype-in-tuberous-sclerosis-patients-with-a-codon-905-missense-mutation-in-the-tsc2-gene(1ce9e366-6bfb-433c-a9de-173b840a3f4b).html
https://biblio.vub.ac.be/vubir/mild-phenotype-in-tuberous-sclerosis-patients-with-a-codon-905-missense-mutation-in-the-tsc2-gene(1ce9e366-6bfb-433c-a9de-173b840a3f4b).html
Autor:
Anna Jansen, Sancak, O., D Agostino, M. D., Badhwar, A., Roberts, P., Gobbi, G., Wilkinson, R., Melanson, D., Koenekoop, R., Gans, M., Den Ouweland, A. M. W., Nellist, M., Pandolfo, M., Sims, K., Thiele, E., Andermann, F., Dubeau, F., Kwiatkowski, D., Halley, D. J. J., Andermann, E.
Publikováno v:
ResearcherID
Purpose: To report the epilepsy phenotype, the clinical manifestations, and functional aspects of codon 905 mutations in tuberous sclerosis type 2 (TSC2). Methods: We carried out a detailed study of the TSC phenotype in a large French-Canadian family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::75e951b409249f548682c55c9709261b
https://biblio.vub.ac.be/vubir/mild-epilepsy-phenotype-in-tsc2-patients-with-codon-905-mutations(4e13f00b-6c35-48df-a7be-5dee0bcb6001).html
https://biblio.vub.ac.be/vubir/mild-epilepsy-phenotype-in-tsc2-patients-with-codon-905-mutations(4e13f00b-6c35-48df-a7be-5dee0bcb6001).html