المؤلفون: Carter, P.^{Aff1, Aff2}, O’Donoghue, K. J. M., Dworzynski, K., O’Shea, L., Roberts, V., Reeves, T., Bastounis, A.^{Aff1, Aff3}, Mugglestone, M. A.^{Aff1, Aff2}, Fawke, J., Pilling, S.^{Aff1, Aff2, Aff5}

المصدر: BMC Medical Research Methodology. 21(1)

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المؤلفون: Curran, S^{Aff1, ID4001839_cor1}, Powell, J, Neale, B M, Dworzynski, K, Li, T, Murphy, D, Bolton, P F

المصدر: Molecular Psychiatry. 11(8):709-713

المؤلفون: Kuznetsov, L, Dworzynski, K, Davies, M, Overton, C, Guideline Committee, Becker, CM

المساهمون: Becker, C

المصدر: BMJ. 358

مصطلحات موضوعية: Gynecology, medicine.medical_specialty, 030219 obstetrics & reproductive medicine, business.industry, General surgery, Pelvic pain, MEDLINE, Endometriosis, Nice, General Medicine, Disease, Guideline, medicine.disease, Menstruation, 03 medical and health sciences, 0302 clinical medicine, medicine, Observational study, 030212 general & internal medicine, medicine.symptom, business, computer, computer.programming_language

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3220fcd46021c616d3ff669747602bbe
http://ora.ox.ac.uk/objects/uuid:

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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

المؤلفون: Simpson, Nuala H, Ceroni, Fabiola, Reader, Rose H, Covill, Laura E, Knight, Julian C, Nudel, R, Monaco, A P, Simonoff, E, Bolton, P F, Pickles, A, Slonims, V, Dworzynski, K, Everitt, A, Clark, A, Watson, J, Seckl, J, Cowie, H, Cohen, W, Nasir, Jamal, Bishop, D V M, Simkin, Z, Hennessy, Elizabeth R, Bolton, Patrick F, Conti-Ramsden, Gina, O'Hare, Anne, Baird, Gillian, Fisher, Simon E, Newbury, Dianne F

المصدر: 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, Bolton, P F, 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 2015, ' Genome-wide analysis identifies a role for common copy number variants in specific language impairment ', European journal of human genetics : EJHG, vol. 23, no. 10, pp. 1370-1377 . https://doi.org/10.1038/ejhg.2014.296

مصطلحات موضوعية: RZ, A100, QH426

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::82e6936c4f6efe1d1b8b76790816c347
https://strathprints.strath.ac.uk/55421/1/Simpson_etal_EJHG_2016_Genome_wide_analysis_identifies_a_role_for_common_copy_number_variants_in_specific.pdf

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