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: Sinars, Daniel B., Scott, Kim C. N., Olson, Russ T., Edwards, M. John

وصف الملف: application/pdf

العلاقة: http://www.osti.gov/servlets/purl/1562853Test; https://www.osti.gov/biblio/1562853Test; https://doi.org/10.2172/1562853Test

الإتاحة: https://doi.org/10.2172/1562853Test
http://www.osti.gov/servlets/purl/1562853Test
https://www.osti.gov/biblio/1562853Test

المؤلفون: Kim, C. N.

المصدر: Journal of Hydrodynamics ; volume 30, issue 6, page 1134-1142 ; ISSN 1001-6058 1878-0342

مصطلحات موضوعية: Mechanical Engineering, Mechanics of Materials, Condensed Matter Physics, Modeling and Simulation

الإتاحة: https://doi.org/10.1007/s42241-018-0142-2Test

المؤلفون: Luo, Yang, Zhu, Mengqi, Kim, C. N.

المصدر: Journal of Hydrodynamics ; volume 30, issue 5, page 920-927 ; ISSN 1001-6058 1878-0342

مصطلحات موضوعية: Mechanical Engineering, Mechanics of Materials, Condensed Matter Physics, Modeling and Simulation

الإتاحة: https://doi.org/10.1007/s42241-018-0109-3Test

المؤلفون: Wen, M. M., Kim, C. N.

المصدر: Journal of Hydrodynamics ; volume 29, issue 4, page 668-678 ; ISSN 1001-6058 1878-0342

مصطلحات موضوعية: Mechanical Engineering, Mechanics of Materials, Condensed Matter Physics, Modeling and Simulation

الإتاحة: https://doi.org/10.1016/s1001-6058Test(16)60778-3
http://api.elsevier.com/content/article/PII:S1001605816607783?httpAccept=text/xmlTest
http://api.elsevier.com/content/article/PII:S1001605816607783?httpAccept=text/plainTest

المؤلفون: Luo, Y., Kim, C. N., Zhu, M. Q.

المصدر: Journal of Hydrodynamics ; volume 29, issue 2, page 332-343 ; ISSN 1001-6058 1878-0342

مصطلحات موضوعية: Mechanical Engineering, Mechanics of Materials, Condensed Matter Physics, Modeling and Simulation

الإتاحة: https://doi.org/10.1016/s1001-6058Test(16)60743-6
http://api.elsevier.com/content/article/PII:S1001605816607436?httpAccept=text/xmlTest
http://api.elsevier.com/content/article/PII:S1001605816607436?httpAccept=text/plainTest

المؤلفون: Park, J S, Kim, N K, Kim, S H, Lee, K Y, Shin, J Y, Kim, C N, Choi, G-S

المساهمون: National Research Foundation of Korea (NRF) Grant funded by the Korean Government (MEST)

المصدر: British Journal of Surgery ; volume 102, issue 12, page 1567-1573 ; ISSN 0007-1323 1365-2168

الإتاحة: https://doi.org/10.1002/bjs.9914Test
http://academic.oup.com/bjs/article-pdf/102/12/1567/36336429/bjs9914.pdfTest

المؤلفون: Park, J. K., Nguyen, T. H., Kim, C. N., Lee, S. Y.

المصدر: International Journal of Automotive Technology ; volume 15, issue 3, page 361-367 ; ISSN 1229-9138 1976-3832

مصطلحات موضوعية: Automotive Engineering

الإتاحة: https://doi.org/10.1007/s12239-014-0038-2Test

المؤلفون: Karagozian, A. R, Nguyen, T. T, Kim, C. N

المصدر: Journal of Propulsion and Power. 2

مصطلحات موضوعية: Fluid Mechanics And Heat Transfer

الوصول الحر: https://ntrs.nasa.gov/citations/19860061580Test