المؤلفون: Williamson KA, Hall HN, Owen LJ, Livesey BJ, Hanson IM, Adams GGW, Bodek S, Calvas P, Castle B, Clarke M, Deng AT, Edery P, Fisher R, Gillessen-Kaesbach G, Heon E, Hurst J, Josifova D, Lorenz B, McKee S, Meire F, Moore AT, Parker M, Reiff CM, Self J, Tobias ES, Verheij JBGM, Willems M, Williams D, van Heyningen V, Marsh JA, FitzPatrick DR

المصدر: Genetics in Medicine, 2019

وصف الملف: application/pdf

الإتاحة: https://eprint.ncl.ac.uk/fulltext.aspx?url=261854/4D0A5D47-CE9D-443F-9DDE-63EAC69E3F81.pdf&pub_id=261854Test

المؤلفون: Tan, K.E.W.P., Meire, F.

المصدر: Kindergeneeskunde voor kinderverpleegkundigen ; page 845-860 ; ISBN 9789036818506 9789036818513

الإتاحة: https://doi.org/10.1007/978-90-368-1851-3_27Test

المؤلفون: Kohl, S., Coppieters, F., Meire, F., Schaich, S., Roosing, S., Brennenstuhl, C., Bolz, S., Genderen, M.M. van, Riemslag, F.C., Lukowski, R., Hollander, A.I. den, Cremers, F.P.M., Baere, E. de, Hoyng, C.B., Wissinger, B.

المصدر: American Journal of Human Genetics, 91, 3, pp. 527-532

مصطلحات موضوعية: NCMLS 6: Genetics and epigenetic pathways of disease, NCMLS 6: Genetics and epigenetic pathways of disease IGMD 3: Genomic disorders and inherited multi-system disorders, NCEBP 2: Evaluation of complex medical interventions IGMD 3: Genomic disorders and inherited multi-system disorders

العلاقة: http://hdl.handle.net/2066/110258Test; https://doi.org/10.1016/j.ajhg.2012.07.006Test

الإتاحة: https://doi.org/10.1016/j.ajhg.2012.07.006Test
http://hdl.handle.net/2066/110258Test

المؤلفون: Estrada-Cuzcano, A., Koenekoop, R.K., Coppieters, F., Kohl, S., Lopez, I., Collin, R.W.J., Baere, E.B. De, Roeleveld, D., Marek, J., Bernd, A., Rohrschneider, K., Born, L.I. van den, Meire, F., Maumenee, I.H., Jacobson, S.G., Hoyng, C.B., Zrenner, E., Cremers, F.P.M., Hollander, A.I. den

المصدر: Investigative Ophthalmology and Visual Science, 52, 2, pp. 834-9

مصطلحات موضوعية: NCMLS 6: Genetics and epigenetic pathways of disease, NCMLS 6: Genetics and epigenetic pathways of disease IGMD 3: Genomic disorders and inherited multi-system disorders, NCEBP 2: Evaluation of complex medical interventions IGMD 3: Genomic disorders and inherited multi-system disorders

العلاقة: http://hdl.handle.net/2066/97979Test; https://doi.org/10.1167/iovs.10-5221Test

الإتاحة: https://doi.org/10.1167/iovs.10-5221Test
http://hdl.handle.net/2066/97979Test

المؤلفون: De Laey, J. J., Meire, F.

المصدر: Documenta Ophthalmologica Proceedings Series ; Retinal Pigment Epithelium and Macular Diseases ; page 285-290 ; ISSN 0303-6405 ; ISBN 9789401061605 9789401151375

الإتاحة: https://doi.org/10.1007/978-94-011-5137-5_47Test

المؤلفون: Ijzer, Suzanne, Leroy, B.P., Baere, E. de, Ravel, T.J. de, Zonneveld-Vrieling, M.N., Voesenek, K.E.J., Kellner, U., Ciriano, J.P., Faber, J.T. de, Rohrschneider, K., Roepman, R., Hollander, A.I. den, Cruysberg, J.R.M., Meire, F., Casteels, I., Moll-Ramirez, N.G. van, Allikmets, R., Born, L.I. van den, Cremers, F.P.M.

المصدر: Investigative Ophthalmology and Visual Science, 47, 3, pp. 1167-76

مصطلحات موضوعية: DCN 1: Perception and Action, IGMD 3: Genomic disorders and inherited multi-system disorders, IGMD 9: Renal disorder, NCMLS 6: Genetics and epigenetic pathways of disease, UMCN 3.3: Neurosensory disorders

العلاقة: https://repository.ubn.ru.nl//bitstream/handle/2066/50548/50548.pdfTest; http://hdl.handle.net/2066/50548Test

الإتاحة: https://doi.org/10.1167/iovs.05-0848Test
http://hdl.handle.net/2066/50548Test
https://repository.ubn.ru.nl//bitstream/handle/2066/50548/50548.pdfTest

المؤلفون: Maugeri, A., Meire, F., Hoyng, C.B., Vink, C.W., Regemorter, N. van, Karan, G., Yang, Z., Cremers, F.P.M., Zhang, K.

المصدر: Investigative Ophthalmology and Visual Science, 45, 12, pp. 4263-7

مصطلحات موضوعية: UMCN 3.3: Neurosensory disorders

العلاقة: http://hdl.handle.net/2066/57144Test

الإتاحة: https://doi.org/10.1167/iovs.04-0078Test
http://hdl.handle.net/2066/57144Test

المؤلفون: Boonstra, F.N., Claerhout, I., Hol, F.A., Smit, G.P., Collenburg, J.J.M. van, Meire, F.

المصدر: Ophthalmic Genetics, 23, 4, pp. 247-51

مصطلحات موضوعية: Elucidation of hereditary disorders and their molecular diagnosis, Opheldering van erfelijke ziekten en hun moleculaire diagnostiek

العلاقة: http://hdl.handle.net/2066/186527Test

الإتاحة: http://hdl.handle.net/2066/186527Test

المؤلفون: De Bleecker, Jan, MEIRE, F, De Reuck, Jacques

المصدر: journal of neurological sciences

مصطلحات موضوعية: Medicine and Health Sciences

العلاقة: https://biblio.ugent.be/publication/391591Test; http://hdl.handle.net/1854/LU-391591Test

الإتاحة: https://biblio.ugent.be/publication/391591Test
http://hdl.handle.net/1854/LU-391591Test

المؤلفون: Assink, JJM (Jacqueline), de Backer, E, Brink, JB, Kohno, T, de Jong, PTVM (Paulus), Bergen, AAB, Meire, F

المصدر: Assink , JJM , de Backer , E , Brink , JB , Kohno , T , de Jong , PTVM , Bergen , AAB & Meire , F 2000 , ' Sorsby fundus dystrophy without a mutation in the TIMP-3 gene ' , British Journal of Ophthalmology , vol. 84 , no. 7 , pp. 679-680 . https://doi.org/10.1136/bjo.84.7.682Test

الإتاحة: https://doi.org/10.1136/bjo.84.7.682Test
https://pure.eur.nl/en/publications/e86dad9c-0a8a-4804-9470-a211f45a9496Test
http://hdl.handle.net/1765/55699Test