المؤلفون: Singh, R. P.^Aff1, Fassnacht, D.^Aff2, Perani, A.^Aff1, Simpson, N. H.^Aff1, Goldenzon, C.^Aff1, Pörtner, R.^Aff2, Al-Rubeai, M.^Aff1

المساهمون: Merten, Otto-Wilhelm, editor, Perrin, Pierre, editor, Griffiths, Bryan, editor

المصدر: New Developments and New Applications in Animal Cell Technology : Proceedings of the 15th ESACT Meeting. :235-241

المؤلفون: Pettigrew, K. A., Fajutrao Valles, S. F., Moll, K., Northstone, K., Ring, S., Pennell, C., Wang, C., Leavett, R., Hayiou-Thomas, M. E., Thompson, P., Simpson, N. H., Fisher, S. E., Whitehouse, A. J O, Snowling, M. J., Newbury, D. F., Paracchini, S., Nudel, R., Monaco, A. P., Francks, C., Baird, G., Slonims, V., Dworzynski, K., Bolton, P. F., Simonoff, E., O'Hare, A., Seckl, J., Cowie, H., Clark, A., Watson, J., Nasir, J., Cohen, W., Everitt, A., Hennessy, E. R., Shaw, D., Helms, P. J., Simkin, Z., Conti, G., Ramsden, D., Bishop, D. V M, Pickles, A.

مصطلحات موضوعية: RM

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::e21fcf510e07074fb271fd3fb7edea4d
https://strathprints.strath.ac.uk/53033/1/Pettigrew_etal_GBB_2015_Lack_of_replication_for_the_myosin_18B_association_with_mathematical.pdf

المؤلفون: Pettigrew, K. A., Reeves, E., Leavett, R., Hayious-Thomas, Emma, Sharma, A., Simpson, N. H., Martinelli, A., Thompson, Paul A., Hulme, Charles, Snowling, Margaret J., Newbury, D. F., Paracchini, S.

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3651::0290a224154e857b2bd481fc95b639bf
https://acuresearchbank.acu.edu.au/item/8qx7x/copy-number-variation-screen-identifies-a-rare-de-novo-deletion-at-chromosome-15q13-1-13-3-in-a-child-with-language-impairment

المؤلفون: Simpson N. H., Ceroni F., Reader R. H., Covill L. E., Knight J. C., Hennessy E. R., Bolton P. F., Conti-Ramsden G., O'Hare A., Baird G., Fisher S. E., Newbury D. F., Nudel R., Monaco A. P., Simonoff E., Pickles A., Slonims V., Dworzynski K., Everitt A., Clark A., Watson J., Seckl J., Cowie H., Cohen W., Nasir J., Bishop D. V. M., Simkin Z.

المساهمون: Simpson N.H., Ceroni F., Reader R.H., Covill L.E., Knight J.C., Nudel R., Monaco A.P., Simonoff E., Pickles A., Slonims V., Dworzynski K., Everitt A., Clark A., Watson J., Seckl J., Cowie H., Cohen W., Nasir J., Bishop D.V.M., Simkin Z, Hennessy E.R., Bolton P.F., Conti-Ramsden G., O'Hare A., Baird G., Fisher S.E., Newbury D.F.

المصدر: European Journal of Human Genetics

مصطلحات موضوعية: Male, Language Disorders, Genome, DNA Copy Number Variations, Specific Language Impairment, Polymorphism, Single Nucleotide, Article, Copy Number Variations, Case-Control Studies, Humans, Female, Genetic Predisposition to Disease, Aged, Genome-Wide Association Study, Language

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8d60e84bcb5b946a4c3d402f5d2fc50d
https://pubmed.ncbi.nlm.nih.gov/25585696

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المؤلفون: Simpson, N. H., Singh, R. P., Emery, A. N., Al-Rubeai, M.

المصدر: Biotechnology & Bioengineering; Jul1999, Vol. 64 Issue 2, p174-186, 13p

المؤلفون: Simpson, N. H., Singh, R. P., Perani, A., Goldenzon, C., Al-Rubeai, M.

المصدر: Biotechnology & Bioengineering; Jul1998, Vol. 59 Issue 1, p90-98, 9p

المؤلفون: Simpson, N. H., Singh, R. P., Emery, A. N., Al-Rubeai, M.

المصدر: Biotechnology & Bioengineering; 20 July 1999, Vol. 64 Issue: 2 p174-186, 13p

المؤلفون: Simpson, N. H., Singh, R. P., Perani, A., Goldenzon, C., Al-Rubeai, M.

المصدر: Biotechnology & Bioengineering; 5 July 1998, Vol. 59 Issue: 1 p90-98, 9p