المؤلفون: Gillentine, M. A., Wang, T., Hoekzema, K., Rosenfeld, J., Liu, P., Guo, H., Kim, C. N., De Vries, B. B. A., Vissers, L. E. L. M., Nordenskjold, M., Kvarnung, M., Lindstrand, A., Nordgren, A., Gecz, J., Iascone, M., Cereda, A., Scatigno, A., Maitz, S., Zanni, G., Bertini, E., Zweier, C., Schuhmann, S., Wiesener, A., Pepper, M., Panjwani, H., Torti, E., Abid, F., Anselm, I., Srivastava, S., Atwal, P., Bacino, C. A., Bhat, G., Cobian, K., Bird, L. M., Friedman, J., Wright, M. S., Callewaert, B., Petit, Florence, Mathieu, S., Afenjar, A., Christensen, C. K., White, K. M., Elpeleg, O., Berger, I., Espineli, E. J., Fagerberg, C., Brasch-Andersen, C., Hansen, L. K., Feyma, T., Hughes, S., Thiffault, I., Sullivan, B., Yan, S., Keller, K., Keren, B., Mignot, C., Kooy, F., Meuwissen, M., Basinger, A., Kukolich, M., Philips, M., Ortega, L., Drummond-Borg, M., Lauridsen, M., Sorensen, K., Lehman, A., Lopez-Rangel, E., Levy, P., Lessel, D., Lotze, T., Madan-Khetarpal, S., Sebastian, J., Vento, J., Vats, D., Benman, L. M., Mckee, S., Mirzaa, G. M., Muss, C., Pappas, J., Peeters, H., Romano, C., Elia, M., Galesi, O., Simon, M. E. H., Van Gassen, K. L. I., Simpson, K., Stratton, R., Syed, S., Thevenon, J., Palafoll, I. V., Vitobello, A., Bournez, M., Faivre, L., Xia, K., Earl, R. K., Nowakowski, T., Bernier, R. A., Eichler, E. E.

المساهمون: Université de Lille, CHU Lille, Washington University School of Medicine Saint Louis, MO, Karolinska University Hospital Solna, Sweden KUH, Maladies Rares du Développement : Génétique, Régulation et Protéomique (RADEME) - ULR 7364, Centre de Référence Déficiences Intellectuelles de causes rares / Rare Disease Reference Center for Intellectual Disability CHU Robert Debré, AP-HP

مصطلحات موضوعية: Gene families, hnRNPs, Neurodevelopmental disorders, Cortex development

وصف الملف: application/octet-stream; application/rdf+xml; charset=utf-8; application/pdf

العلاقة: Genome Medicine; Genome Med; http://hdl.handle.net/20.500.12210/84177Test

الإتاحة: https://doi.org/20.500.12210/84177Test
https://hdl.handle.net/20.500.12210/84177Test

المؤلفون: Gillentine, M. A., Wang, T., Hoekzema, K., Rosenfeld, J., Liu, P., Guo, H., Kim, C. N., de Vries, B. B. A., Vissers, L. E. L. M., Nordenskjold, M., Kvarnung, M., Lindstrand, A., Nordgren, A., Gecz, J., Iascone, M., Cereda, A., Scatigno, A., Maitz, S., Zanni, G., Bertini, E., Zweier, C., Schuhmann, S., Wiesener, A., Pepper, M., Panjwani, H., Torti, E., Abid, F., Anselm, I., Srivastava, S., Atwal, P., Bacino, C. A., Bhat, G., Cobian, K., Bird, L. M., Friedman, J., Wright, M. S., Callewaert, B., Petit, Florence, Mathieu, S., Afenjar, A., Christensen, C. K., White, K. M., Elpeleg, O., Berger, I., Espineli, E. J., Fagerberg, C., Brasch-Andersen, C., Hansen, L. K., Feyma, T., Hughes, S., Thiffault, I., Sullivan, B., Yan, S., Keller, K., Keren, B., Mignot, C., Kooy, F., Meuwissen, M., Basinger, A., Kukolich, M., Philips, M., Ortega, L., Drummond-Borg, M., Lauridsen, M., Sorensen, K., Lehman, A., Lopez-Rangel, E., Levy, P., Lessel, D., Lotze, T., Madan-Khetarpal, S., Sebastian, J., Vento, J., Vats, D., Benman, L. M., Mckee, S., Mirzaa, G. M., Muss, C., Pappas, J., Peeters, H., Romano, C., Elia, M., Galesi, O., Simon, M. E. H., van Gassen, K. L. I., Simpson, K., Stratton, R., Syed, S., Thevenon, J., Palafoll, I. V., Vitobello, A., Bournez, M., Faivre, L., Xia, K., Earl, R. K., Nowakowski, T., Bernier, R. A., Eichler, E. E.

المساهمون: Washington University School of Medicine Saint Louis, MO, Karolinska University Hospital Solna, Sweden (KUH), Maladies RAres du DEveloppement embryonnaire et du MEtabolisme : du Phénotype au Génotype et à la Fonction - ULR 7364 (RADEME), Université de Lille-Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille), Centre de Référence Déficiences Intellectuelles de causes rares / Rare Disease Reference Center for Intellectual Disability CHU Robert Debré, AP-HP, AP-HP Hôpital universitaire Robert-Debré Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)

المصدر: ISSN: 1756-994X ; Genome Medicine ; https://hal.univ-lille.fr/hal-04219731Test ; Genome Medicine, 2021, Genome Medicine, 13 (63), ⟨10.1186/s13073-021-00870-6⟩.

مصطلحات موضوعية: Gene families, Cortex development, hnRNPs, Neurodevelopmental disorders, [SDV]Life Sciences [q-bio]

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33874999; hal-04219731; https://hal.univ-lille.fr/hal-04219731Test; https://hal.univ-lille.fr/hal-04219731/documentTest; https://hal.univ-lille.fr/hal-04219731/file/s13073-021-00870-6.pdfTest; PUBMED: 33874999

الإتاحة: https://doi.org/10.1186/s13073-021-00870-6Test
https://hal.univ-lille.fr/hal-04219731Test
https://hal.univ-lille.fr/hal-04219731/documentTest
https://hal.univ-lille.fr/hal-04219731/file/s13073-021-00870-6.pdfTest

المؤلفون: Wright, M. S.

مصطلحات موضوعية: 615.5

الإتاحة: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664043Test

المؤلفون: Wright, M. S., Covich, A. P.

المصدر: Microbial Ecology, 2005 May 01. 49(4), 536-546.

الوصول الحر: https://www.jstor.org/stable/25153208Test

المؤلفون: Bruhn, K. W., Pantapalangkoor, P., Nielsen, T., Tan, B., Junus, J., Hujer, K. M., Wright, M. S., Bonomo, R. A., Adams, M. D., Chen, W., Spellberg, B.

المصدر: Journal of Infectious Diseases ; ISSN 0022-1899 1537-6613

مصطلحات موضوعية: Infectious Diseases, Immunology and Allergy

الإتاحة: https://doi.org/10.1093/infdis/jiu593Test
http://academic.oup.com/jid/article-pdf/211/8/1296/5084443/jiu593.pdfTest

المؤلفون: Wollen, E J, Wright, M S, Gunther, C -C, Bik-Multanowski, M, Madetko-Talowska, A, Sejersted, Y, Kwinta, P, Pietrzyk, J J, Saugstad, O D

المصدر: Pediatric Research ; volume 70, page 223-223 ; ISSN 0031-3998 1530-0447

مصطلحات موضوعية: Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1038/pr.2011.448Test

المؤلفون: Wollen, E J, Sejersted, Y, Wright, M S, Gunther, C C, Pietrzyk, J J, Bik-Multanowski, M, Madetko-Talowska, A, Kwinta, P, Saugstad, O D

المصدر: Pediatric Research ; volume 68, page 180-180 ; ISSN 0031-3998 1530-0447

مصطلحات موضوعية: Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1203/00006450-201011001-00349Test

المؤلفون: Gary W. Phillips, Ph. D, Lynnett Wright M. S

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://assessment.air.org/Papers/PsychometricTest Advances in Alternate Assessments_phillips.pdf.

مصطلحات موضوعية: TABLE OF CONTENTS Executive Summary.

وصف الملف: application/pdf

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.533.7229Test; http://assessment.air.org/Papers/PsychometricTest Advances in Alternate Assessments_phillips.pdf

الإتاحة: http://assessment.air.org/Papers/PsychometricTest Advances in Alternate Assessments_phillips.pdf

المؤلفون: Aresvik, D M, Pettersen, R D, Abrahamsen, T G, Wright, M S

مصطلحات موضوعية: Haematology immunology

وصف الملف: text/html

العلاقة: http://adc.bmj.com/cgi/content/short/93/2_MeetingAbstracts/pw375Test

الإتاحة: http://adc.bmj.com/cgi/content/short/93/2_MeetingAbstracts/pw375Test

المؤلفون: Wright, M. S., Osbrink, W. L. A., Lax, A. R.

المصدر: ACS Symposium Series ; Agricultural Applications in Green Chemistry ; page 173-188 ; ISSN 0097-6156 1947-5918 ; ISBN 9780841238282 9780841219991

الإتاحة: https://doi.org/10.1021/bk-2004-0887.ch012Test