Zobrazeno 1 - 10
of 229
pro vyhledávání: '"Malmgren, H."'
Autor:
Schaetzel, J. Robert, Malmgren, H. B.
Publikováno v:
Foreign Policy, 1980 Jul 01(39), 130-142.
Externí odkaz:
https://www.jstor.org/stable/1148416
Autor:
Malmgren, H. B.
Publikováno v:
The Quarterly Journal of Economics, 1961 Aug 01. 75(3), 399-421.
Externí odkaz:
https://www.jstor.org/stable/1885131
Autor:
Malmgren, H. B.
Publikováno v:
Oxford Economic Papers, 1963 Mar 01. 15(1), 74-79.
Externí odkaz:
https://www.jstor.org/stable/2661771
Autor:
Malmgren, H. B.
Publikováno v:
The Journal of Industrial Economics, 1959 Mar 01. 7(2), 136-144.
Externí odkaz:
https://www.jstor.org/stable/2097689
Autor:
Malmgren, H. B., Schlechty, D. L.
Publikováno v:
American Journal of Agricultural Economics, 1969 Dec 01. 51(5), 1325-1337.
Externí odkaz:
https://www.jstor.org/stable/1238010
Autor:
Araoz, A. B., Malmgren, H. B.
Publikováno v:
The Review of Economic Studies, 1961 Jun 01. 28(3), 202-211.
Externí odkaz:
https://www.jstor.org/stable/2295949
Autor:
Eckerström, C., Olsson, E., Borga, M., Ekholm, S., Ribbelin, S., Rolstad, S., Starck, G., Edman, Å., Wallin, A., Malmgren, H.
Publikováno v:
In Journal of the Neurological Sciences 2008 272(1):48-59
Autor:
Dijck, A. van, Vulto-van Silfhout, A.T., Cappuyns, E., Werf, I.M. van der, Mancini, G.M., Tzschach, A., Bernier, R., Gozes, I., Eichler, E.E., Romano, C., Lindstrand, A., Nordgren, A., Kvarnung, M., Kleefstra, T., Vries, B.B.A. de, Kury, S., Rosenfeld, J.A., Meuwissen, M.E., Vandeweyer, G., Kooy, R.F., Bakshi, M., Wilson, M., Berman, Y., Dickson, R., Fransen, E., Helsmoortel, C., Ende, J. van den, Aa, N. van der, Wijdeven, M.J. van de, Rosenblum, J., Monteiro, F., Kok, F., Quercia, N., Bowdin, S., Dyment, D., Chitayat, D., Alkhunaizi, E., Boonen, S.E., Keren, B., Jacquette, A., Faivre, L., Bezieau, S., Isidor, B., Riess, A., Moog, U., Lynch, S.A., McVeigh, T., Elpeleg, O., Smeland, M.F., Fannemel, M., Haeringen, A. van, Maas, S.M., Veenstra-Knol, H.E., Schouten, M., Willemsen, M.H., Marcelis, C.L., Ockeloen, C., Burgt, I. van der, Feenstra, I., Smagt, J. van der, Jezela-Stanek, A., Krajewska-Walasek, M., Gonzalez-Lamuno, D., Anderlid, B.M., Malmgren, H., Nordenskjold, M., Clement, E., Hurst, J., Metcalfe, K., Mansour, S., Lachlan, K., Clayton-Smith, J., Hendon, L.G., Abdulrahman, O.A., Morrow, E., McMillan, C., Gerdts, J., Peeden, J., Vergano, S.A.S., Valentino, C., Chung, W.K., Ozmore, J.R., Bedrosian-Sermone, S., Dennis, A., Treat, K., Hughes, S.S., Safina, N., Pichon, J.B. le, McGuire, M., Infante, E., Madan-Khetarpal, S., Desai, S., Benke, P., Krokosky, A., Cristian, I., Baker, L., Gripp, K., Stessman, H.A., Eichenberger, J., Jayakar, P., Pizzino, A., Manning, M.A., Slattery, L., ADNP Consortium
Publikováno v:
Biological Psychiatry, 85(4), 287-297. ELSEVIER SCIENCE INC
Biological Psychiatry Volume 85, Issue 4, 15 February 2019, Pages 287-297
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Biological Psychiatry, 85, 4, pp. 287-297
Biological Psychiatry, 85(4), 287. Elsevier USA
Biological psychiatry
Biological Psychiatry, 85, 287-297
Biological psychiatry, 85(4), 287-297. Elsevier USA
Biological Psychiatry, 85(4), 287-297. Elsevier Inc.
Biological Psychiatry Volume 85, Issue 4, 15 February 2019, Pages 287-297
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Biological Psychiatry, 85, 4, pp. 287-297
Biological Psychiatry, 85(4), 287. Elsevier USA
Biological psychiatry
Biological Psychiatry, 85, 287-297
Biological psychiatry, 85(4), 287-297. Elsevier USA
Biological Psychiatry, 85(4), 287-297. Elsevier Inc.
Background In genome-wide screening studies for de novo mutations underlying autism and intellectual disability, mutations in the ADNP gene are consistently reported among the most frequent. ADNP mutations have been identified in children with autism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::517869385daa59216cda03fc628eb520
http://hdl.handle.net/1887/122773
http://hdl.handle.net/1887/122773
Autor:
Bengani, Hemant, Handley, Mark, Alvi, Mohsan, Ibitoye, Rita, Lees, Melissa, Lynch, Sally Ann, Lam, Wayne, Fannemel, Madeleine, Nordgren, Ann, Malmgren, H, Kvarnung, M, Mehta, Sarju, McKee, Shane, Whiteford, Margo, Stewart, Fiona, Connell, Fiona, Clayton-Smith, Jill, Mansour, Sahar, Mohammed, Shehla, Fryer, Alan, Morton, Jenny, UK10K Consortium, Grozeva, Detelina, Asam, Tara, Moore, David, Sifrim, Alejandro, McRae, Jeremy, Hurles, Matthew E, Firth, Helen V, Raymond, F Lucy, Kini, Usha, Nellåker, Christoffer, Ddd Study, FitzPatrick, David R
PURPOSE: To characterize features associated with de novo mutations affecting SATB2 function in individuals ascertained on the basis of intellectual disability. METHODS: Twenty previously unreported individuals with 19 different SATB2 mutations (11 l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::803835aaf0e6c4f6f46870f62a72c8b6
https://openaccess.sgul.ac.uk/id/eprint/109307/1/gim2016211.pdf
https://openaccess.sgul.ac.uk/id/eprint/109307/1/gim2016211.pdf
STUDY QUESTION Has PGD-HLA been successful relative to diagnostic and clinical efficacy? SUMMARY ANSWER The diagnostic efficacy of PGD-HLA protocols was found lower in this study in comparison to published PGD-HLA protocols and to that reported for g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::0625abf2b6341f7e02a1ccd64ac82b44
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3107634
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3107634