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1دورية أكاديمية
المؤلفون: Newbury, D. F., Paracchini, S., Scerri, T. S., Winchester, L., Addis, L., Richardson, Alex J., Walter, J., Stein, J. F., Talcott, J. B., Monaco, A. P.
المصدر: Behavior Genetics: An International Journal Devoted to Research in the Inheritance of Behavior. January 2011 41(1):90-104
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المؤلفون: den Hoed, J., De Boer, E., Voisin, N., Guex, N., Blok, L. Snijders, Chrast, J., Manwaring, L., Willing, M., Waheeb, A., Osmond, M., McWalter, K., Vitobello, A., Demurger, F., Lavillaureix, A., Odent, S., Mazel, B., Faivre, L., Thiffault, I., Schwager, C., Amudhavalli, S. M., Rosenfeld, J. A., Radtke, K., Preiksaitiene, E., Ranza, E., Depienne, C., Kuechler, A., Mohammed, S., Abedi, Y. Hamzavi, Bonagura, V. R., Zuccarelli, B., Horist, B., Krishnamurthy, V., Kattentidt-Mouravieva, A. A., Granger, L., Petersen, A., Jones, K. L., Sinnema, M., Stegmann, A. P. A., Newbury-Ecob, R., Kini, U., Newbury, D. F., Gilissen, C., Brunner, H., Kleefstra, T., Reymond, A., Vissers, L. E. L. M., Fisher, S. E.
المساهمون: Donders Institute for Brain, Cognition and Behaviour, Radboud university [Nijmegen], Université de Lausanne (UNIL), Washington University in Saint Louis (WUSTL), GeneDx [Gaithersburg, MD, USA], Université Bourgogne Franche-Comté [COMUE] (UBFC), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Groupe Hospitalier Bretagne Sud (GHBS), Institut de Génétique et Développement de Rennes (IGDR), Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )-Centre National de la Recherche Scientifique (CNRS)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES), Ambry Genetics [Aliso Viejo, CA, USA], University of Kansas [Lawrence] (KU), Maastricht University [Maastricht], Radboud University [Nijmegen], Université de Lausanne = University of Lausanne (UNIL), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )
المصدر: European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2020, 28 (SUPPL 1), pp.32-33
European Journal of Human Genetics, 2020, 28 (SUPPL 1), pp.32-33مصطلحات موضوعية: [SDV]Life Sciences [q-bio], ComputingMilieux_MISCELLANEOUS
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3دورية أكاديمية
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4دورية أكاديمية
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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
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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 -
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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
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8دورية أكاديمية
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المؤلفون: Newbury, D. F., Ishikawa-Brush, Y., Marlow, A. J., Fisher, S. E., Monaco, A. P., Stott, C. M., Merricks, M. J., Goodyer, I. M., Patrick Bolton, Jannoun, L., Slonims, V., Baird, G., Andrew Pickles, Bishop, D. V. M., Conti-Ramsden, G., Helms, P. J., Sli, Consortium
المصدر: American Journal of Human Genetics
King's College Londonمصطلحات موضوعية: Male, X Chromosome, Adolescent, Genotype, Intelligence, Twins, Nuclear Family, Cohort Studies, Quantitative Trait, Heritable, Diseases in Twins, Humans, Computer Simulation, Genetic Predisposition to Disease, Language Development Disorders, Child, Language Tests, Models, Genetic, Genome, Human, Chromosome Mapping, Articles, Phenotype, England, Child, Preschool, Female, Lod Score, Chromosomes, Human, Pair 19, Chromosomes, Human, Pair 16
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9a604a194b11102c31089dbe91485d99
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=384915&tool=pmcentrez&rendertype=abstract -
10دورية أكاديمية
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