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1دورية أكاديمية
المؤلفون: Poorthuis, B.J.H.M., Wevers, R.A., Kleijer, W.J., Groener, J.E.M., de Jong, J.G.N., van Weely, S., Niezen-Koning, K.E., van Diggelen, O.P.
المصدر: Human Genetics. August 1999 105(1-2):151-156
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2دورية
المؤلفون: Linnebank, M., Semmler, A., Moskau, S., Kleijer, W.J., van der Sterre, M.L.T., Gärtner, J., Fliessbach, K., Sokolowski, P., Köhler, W., Schlegel, U., Klockgether, T., Wanders, R.J.A., Schmidt, S., Wüllner, U., Kemp, S.
المصدر: Aktuelle Neurologie; 20240101, Issue: Preprints
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المؤلفون: Ausems, M.G.E.M., Kroos, M.A., Kraan, M. van der, Smeitink, J.A.M., Kleijer, W.J., Ploos van Amstel, J.K., Reuser, A.J.J.
المصدر: Clinical Genetics, 49, 325-328
Clinical Genetics, 49, pp. 325-328
Clinical Genetics, 49, 6, pp. 325-328مصطلحات موضوعية: Central Nervous System, Pregnancy Complications, Cardiovascular, Inborn errors of metabolism, Cardiovascular, Biochemical, Clinical, Metabolic Diseases, Genetics, Genetics, Biochemical, Neural Tube Defects, Vascular Diseases, Metabolic Processes (Non MeSH), Erfelijke stofwisselingsziekten, Muscle, Skeletal, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries), Hereditary Diseases, Mental Disorders, Inborn Errors, Mitochondrial Myopathies, Skeletal, Neuromuscular Diseases, Fibroblasts, Mitochondria, Pregnancy Complications, Chemistry, Metabolism, Chemistry, Clinical, Mutation, Muscle, Homocystinuria, Energy Metabolism, Metabolism, Inborn Errors
وصف الملف: application/pdf
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المؤلفون: Broeks, A., Veer, L.J. van 't, Ottenheim, C., Hiel, J.A.P., Kleijer, W.J., Weemaes, C.M.R.
المصدر: Nederlands Tijdschrift voor Geneeskunde, 147, 386-9
Nederlands Tijdschrift voor Geneeskunde, 147, 9, pp. 386-9مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Immunotherapy, gene therapy and transplantation [UMCN 1.4], Microbial pathogenesis and host defense [UMCN 4.1]
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::456ee9c268655c213ad3e46feb7cd431
http://hdl.handle.net/2066/144268 -
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المؤلفون: Boehmer, A.L., Brinkmann, A.O., Bruggenwirth, H.T., Assendelft, C. van, Otten, B.J., Verleun-Mooijman, M.C.T., Niermeijer, M.F., Brunner, H.G., Rouwé, C.W., Waelkens, J.J., Oostdijk, W., Kleijer, W.J., Kwast, T.H. van der, Vroede, M.A. de, Drop, S.L.
المصدر: Journal of Clinical Endocrinology and Metabolism, 86, 9, pp. 4151-60
Journal of Clinical Endocrinology and Metabolism, 86, 4151-60مصطلحات موضوعية: Elucidation of hereditary disorders and their molecular diagnosis, Opheldering van erfelijke ziekten en hun moleculaire diagnostiek
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::636ce3b24ed9853c4126245dad4f1661
https://hdl.handle.net/2066/144648 -
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المؤلفون: Vermeulen, W., Rademakers, S., Jaspers, N.G.J., Appeldoorn, E., Raams, A., Klein, B., Kleijer, W.J., Kjærsgaard Hansen, Lars
المصدر: Vermeulen, W, Rademakers, S, Jaspers, N G J, Appeldoorn, E, Raams, A, Klein, B, Kleijer, W J & Kjærsgaard Hansen, L 2001, ' A temperature-sensitive disorder in basal transcription and DNA repair in humans ', Nature Genetics, vol. 27, pp. 299-303 .
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3062::ea04af1a41169494f3694bbe9211e5e8
https://portal.findresearcher.sdu.dk/da/publications/cbb335e0-6fcd-11db-81a9-000ea68e967b -
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المؤلفون: Vervoort, R., Buist, N.R.M., Kleijer, W.J., Wevers, R., Fryns, J.-P., Liebaers, I., Lissens, W.
المصدر: Human Genetics, 99, 462-468
Human Genetics, 99, iss, 4, pp. 462-468وصف الملف: application/pdf
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المؤلفون: Bruggenwirth, H.T., Boehmer, A.L., Verleun-Mooijman, M.C.T., Hoogenboezem, T., Kleijer, W.J., Otten, B.J., Trapman, J., Brinkmann, A.O.
المصدر: Journal of Steroid Biochemistry and Molecular Biology, 5/6, pp. 569-575
Journal of Steroid Biochemistry and Molecular Biology, 5/6, 569-575مصطلحات موضوعية: Overig onderzoek afdeling Paediatrics
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المؤلفون: Kroos, M.A., Kraan, M. van der, Diggelen, O.P. van, Kleijer, W.J., Reuser, A.J.J., Boogaard, M.J. van den, Ausems, M.G.E.M., Ploos van Amstel, J.K., Poenaru, L., Nicolino, M., Wevers, R.A.
المصدر: Journal of Medical Genetics, 32, pp. 836-837
Journal of Medical Genetics, 32, 836-837مصطلحات موضوعية: Lysosomale en neurometabole ziekten, Lysosomal and neurometabolic diseases
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المؤلفون: Eveno, E., Bourre, F., Quilliet, X., Chevallier-Lagente, O., Roza, L., Eker, A.P.M., Kleijer, W.J., Nikaido, O., Stefanini, M., Hoeijmakers, J.H.J., Bootsma, D., Cleaver, J.E., Sarasin, A., Mezzina, M.
المساهمون: Centraal Instituut voor Voedingsonderzoek TNO
المصدر: Cancer Research, 55, 4325-4332
مصطلحات موضوعية: Nutrition
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::fd56037c825a9496b1c39a0188f583ec
http://resolver.tudelft.nl/uuid:5648fbcc-c9d1-4d2d-ac4d-611367c0ae28
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