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1دورية أكاديمية
المؤلفون: Dijk, K.D. van, Darweesh, S.K.L., Heuvel, O.A. van den, Overeem, S., Werf, Y.D. van der, Pijpers, W.
المصدر: Nederlands Tijdschrift voor Geneeskunde, 168
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2دورية أكاديمية
المؤلفون: Baat, C. de, Stiphout, M.A.E. van, Dijk, K.D. van, Berendse, H.W., Verhoeff, M.C., Lobbezoo, F.
المصدر: Nederlands Tijdschrift voor Tandheelkunde, 126, 3, pp. 127-132
مصطلحات موضوعية: Radboudumc 10: Reconstructive and regenerative medicine RIHS: Radboud Institute for Health Sciences
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3دورية أكاديمية
المؤلفون: Simon-Sanchez, J., Hilten, J.J. van, Warrenburg, B.P.C. van de, Post, B., Berendse, H.W., Arepalli, S., Hernandez, D.G., Bie, R.M. de, Velseboer, D., Scheffer, H., Bloem, B.R., Dijk, K.D. van, Rivadeneira, F., Hofman, A., Uitterlinden, A.G., Rizzu, P., Bochdanovits, Z., Singleton, A.B., Heutink, P.
المصدر: European Journal of Human Genetics, 19, 6, pp. 655-61
مصطلحات موضوعية: DCN 2: Functional Neurogenomics, IGMD 3: Genomic disorders and inherited multi-system disorders DCN 2: Functional Neurogenomics
العلاقة: http://hdl.handle.net/2066/96958Test
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4دورية أكاديمية
المؤلفون: Plagnol, V., Nalls, M.A., Bras, J.M., Hernandez, D., Sharma, M., Sheerin, U.M., Saad, M., Simon-Sanchez, J., Schulte, C., Lesage, S., Sveinbjornsdottir, S., Amouyel, P., Arepalli, S., Band, G., Barker, R.A., Bellinguez, C., Ben-Shlomo, Y., Berendse, H.W., Berg, D., Bhatia, K.P., Bie, R.M. de, Biffi, A., Bloem, B.R., Bochdanovits, Z., Bonin, M., Brockmann, K., Brooks, J., Burn, D.J., Charlesworth, G., Chen, H., Chinnery, P.F., Chong, S., Clarke, C.E., Cookson, M.R., Cooper, J.M., Corvol, J.C., Counsell, J., Damier, P., Dartigues, J.F., Deloukas, P., Deuschl, G., Dexter, D.T., Dijk, K.D. van, Dillman, A., Durif, F., Durr, A., Edkins, S., Evans, J.R., Foltynie, T., Freeman, C., Gao, J., Gardner, M., Gibbs, J.R., Goate, A., Gray, E., Guerreiro, R., Gustafsson, O., Harris, C., Hellenthal, G., Hilten, J.J. van, Hofman, A., Hollenbeck, A., Holton, J.L., Hu, M., Huang, X., Huber, H, Hudson, G., Hunt, S.E., Huttenlocher, J., Illig, T., Jonsson, P.V., Langford, C., Lees, A.J., Lichtner, P., Limousin, P., Lopez, G., McNeill, A., Moorby, C., Moore, M., Morris, H.A., Morrison, K.E., Mudanohwo, E., O'Sullivan, S.S, Pearson, J., Pearson, R., Perlmutter, J., Petursson, H., Pirinen, M., Polnak, P., Post, B., Potter, S.C., Ravina, B., Revesz, T., Riess, O., Rivadeneira, F., Rizzu, P., Ryten, M., Sawcer, S.J., Schapira, A., Scheffer, H., Shaw, K., Shoulson, I., Sidransky, E., Silva, R. de, Smith, C., Spencer, C.C., Stefansson, H., Steinberg, S., Stockton, J.D., Strange, A., Su, Z., Talbot, K., Tanner, C.M., Tashakkori-Ghanbaria, A., Tison, F., Trabzuni, D., Traynor, B.J., Uitterlinden, A.G., Vandrovcova, J., Velseboer, D., Vidailhet, M., Vukcevic, D., Walker, R., Warrenburg, B.P.C. van de, Weale, M.E., Wickremaratchi, M., Williams, N., Williams-Gray, C.H., Winder-Rhodes, S., Stefansson, K., Martinez, M., Donnelly, P., Singleton, A.B., Hardy, J., Heutink, P., Brice, A., Gasser, T., Wood, N.W.
المصدر: Plos Genetics, 7, 6, pp. e1002142-e1002142
مصطلحات موضوعية: DCN 2: Functional Neurogenomics, DCN 2: Functional Neurogenomics NCEBP 10: Human Movement & Fatigue, IGMD 3: Genomic disorders and inherited multi-system disorders DCN 2: Functional Neurogenomics
العلاقة: https://repository.ubn.ru.nl//bitstream/handle/2066/97597/97597.pdfTest; http://hdl.handle.net/2066/97597Test
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5دورية أكاديمية
المؤلفون: Nalls, M.A., Plagnol, V., Hernandez, D.G., Sharma, M., Sheerin, U.M., Saad, M., Simon-Sanchez, J., Schulte, C., Lesage, S., Sveinbjornsdottir, S., Arepalli, S., Barker, R., Ben-Shlomo, Y., Berendse, H.W., Berg, D., Bhatia, K., Bie, R.M.A. de, Biffi, A., Bloem, B., Bochdanovits, Z., Bonin, M., Bras, J.M., Brockmann, K., Brooks, J., Burn, D.J., Charlesworth, G., Chen, H.L., Chinnery, P.F., Chong, S., Clarke, C.E., Cookson, M.R., Cooper, J.M., Corvol, J.C., Counsell, C., Damier, P., Dartigues, J.F., Deloukas, P., Deuschl, G., Dexter, D.T., Dijk, K.D. van, Dillman, A., Durif, F., Durr, A., Edkins, S., Evans, J.R., Foltynie, T., Gao, J.J., Gardner, M., Gibbs, J.R., Goate, A., Gray, E., Guerreiro, R., Gustafsson, O., Harris, C., Hilten, J.J. van, Hofman, A., Hollenbeck, A., Holton, J., Hu, M., Huang, X.M., Huber, H., Hudson, G., Hunt, S.E., Huttenlocher, J., Illig, T., Jonsson, P.V., Lambert, J.C., Langford, C., Lees, A., Lichtner, P., Limousin, P., Lopez, G., Lorenz, D., McNeill, A., Moorby, C., Moore, M., Morris, H.R., Morrison, K.E., Mudanohwo, E., O'Sullivan, S.S., Pearson, J., Perlmutter, J.S., Petursson, H., Pollak, P., Post, B., Potter, S., Ravina, B., Revesz, T., Riess, O., Rivadeneira, F., Rizzu, P., Ryten, M., Sawcer, S., Schapira, A., Scheffer, H., Shaw, K., Shoulson, I., Sidransky, E., Smith, C., Spencer, C.C.A., Stefansson, H., Stockton, J.D., Strange, A., Talbot, K., Tanner, C.M., Tashakkori-Ghanbaria, A., Tison, F., Trabzuni, D., Traynor, B.J., Uitterlinden, A.G., Velseboer, D., Vidailhet, M., Walker, R., Warrenburg, B. van de, Wickremaratchi, M., Williams, N., Williams-Gray, C.H., Winder-Rhodes, S., Stefansson, K., Martinez, M., Hardy, J., Heutink, P., Brice, A., Gasser, T., Singleton, A.B., Wood, N.W., Int Parkinson Dis Genomics Consort, Wellcome Trust Case-Control Consor
المصدر: Lancet
العلاقة: lumc-id: 3848116; https://hdl.handle.net/1887/103793Test
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6دورية أكاديمية
المؤلفون: Reesink, F.E., Lemstra, A.W., Dijk, K.D. van, Berendse, H.W., Berg, W.D. van de, Klein, M., Blankenstein, M.A., Scheltens, P., Verbeek, M.M., Flier, W.M. van der
المصدر: Journal of Alzheimer's Disease, 22, 1, pp. 87-95
مصطلحات موضوعية: DCN 2: Functional Neurogenomics, DCN 3: Neuroinformatics
العلاقة: https://repository.ubn.ru.nl//bitstream/handle/2066/88288/88288.pdfTest; http://hdl.handle.net/2066/88288Test
الإتاحة: https://doi.org/10.3233/JAD-2010-100186Test
http://hdl.handle.net/2066/88288Test
https://repository.ubn.ru.nl//bitstream/handle/2066/88288/88288.pdfTest
