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51دورية أكاديمية
المؤلفون: Heinen, CA, Losekoot, M, Sun, Y, Watson, P J, Fairall, L, Joustra, SD, Zwaveling-Soonawala, N, Oostdijk, W (Wilma), van den Akker, Erica, Alders, M, Santen, GWE, van Rijn, RR, Dreschler, WA, Surovtseva, O V, Biermasz, NR, Hennekam, RC, Wit, JM, Schwabe, J W R, Boelen, A, Fliers, E, van Trotsenburg, ASP
المصدر: Heinen , CA , Losekoot , M , Sun , Y , Watson , P J , Fairall , L , Joustra , SD , Zwaveling-Soonawala , N , Oostdijk , W , van den Akker , E , Alders , M , Santen , GWE , van Rijn , RR , Dreschler , WA , Surovtseva , O V , Biermasz , NR , Hennekam , RC , Wit , JM , Schwabe , J W R , Boelen , A , Fliers , E & van Trotsenburg , ASP 2016 , ' Mutations in TBL1X Are Associated ....
وصف الملف: application/pdf
الإتاحة: https://doi.org/10.1210/jc.2016-2531Test
https://pure.eur.nl/en/publications/a2c1baa2-e11c-4cf8-9596-610458d5ecbbTest
https://pure.eur.nl/ws/files/47714691/REPUB_94856_OA.pdfTest
http://hdl.handle.net/1765/94856Test -
52دورية أكاديمية
المؤلفون: Wilde, A.A., Moss, A.J., Kaufman, E.S., Shimizu, W., Peterson, D.R., Benhorin, J., Lopes, C., Towbin, J.A., Spazzolini, C., Crotti, L., Zareba, W., Goldenberg, I., Kanters, J.K., Robinson, J.L., Qi, M., Hofman, N., Tester, D.J., Bezzina, C.R., Alders, M., Aiba, T., Kamakura, S., Miyamoto, Y., Andrews, M.L., McNitt, S., Polonsky, B., Schwartz, P.J., Ackerman, M.J.
المصدر: Circulation 134, 872-882 (2016)
مصطلحات موضوعية: Scn5a, Genetic Testing, Long Qt Syndrome, Risk Stratification, Sudden Cardiac Death, Arrhythmia
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27566755; info:eu-repo/semantics/altIdentifier/wos/undefined; info:eu-repo/semantics/altIdentifier/isbn/0009-7322; info:eu-repo/semantics/al; https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=49332Test; urn:isbn:0009-7322; urn:issn:0009-7322; urn:issn:1524-4539
الإتاحة: https://doi.org/10.1161/CIRCULATIONAHA.116.021823Test
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=49332Test -
53مؤتمر
المؤلفون: Aref-Eshghi, E., Kerkhof, J., Pedro, V., DI France, Groupe, Barat-Houari, M., Ruiz-Pallares, N., Alders, M., Mannens, M., Henneman, P., Hennekam, R.C., Ciolf, A., Pizzi, S., Tartaglia, M., Campeau, P.M., Rousseau, J., Levy, M.A., Brick, L., Kozenko, M., Balci, T.B., Siu, V.M., Stuart, A., Kadour, M., Masters, J., Takano, K., Kleefstra, T., de Leeuw, N., Field, M., Shaw, M., Gecz, J., Merla, G., Ainsworth, P.J., Lin, H., Rodenhiser, D.I., Friez, M.J., Tedder, M., DuPont, J.A., Stevenson, R.E., Skinner, S.A., Schwartz, C.E., Genevieve, D., Sadikovic, B.
المصدر: Paediatrics Publications
وصف الملف: application/pdf
العلاقة: https://ir.lib.uwo.ca/paedpub/553Test; https://ir.lib.uwo.ca/context/paedpub/article/1560/viewcontent/s41431_020_00740_6.pdfTest
الإتاحة: https://doi.org/10.1038/s41431-020-00740-6Test
https://ir.lib.uwo.ca/paedpub/553Test
https://ir.lib.uwo.ca/context/paedpub/article/1560/viewcontent/s41431_020_00740_6.pdfTest -
54دورية أكاديمية
المؤلفون: Wyrwoll, M. J., van Walree, E. S., Hamer, G., Rotte, N., Motazacker, M. M., Meijers-Heijboer, H., Alders, M., Meißner, A., Kaminsky, E., Wöste, M., Krallmann, C., Kliesch, S., Hunt, T. J., Clark, A. T., Silber, S., Stallmeyer, B., Friedrich, C., van Pelt, A. M. M., Mathijssen, I. B., Tüttelmann, F.
المصدر: Wyrwoll , M J , van Walree , E S , Hamer , G , Rotte , N , Motazacker , M M , Meijers-Heijboer , H , Alders , M , Meißner , A , Kaminsky , E , Wöste , M , Krallmann , C , Kliesch , S , Hunt , T J , Clark , A T , Silber , S , Stallmeyer , B , Friedrich , C , van Pelt , A M M , Mathijssen , I B & Tüttelmann , F 2021 , ' Bi-allelic variants in DNA mismatch repair proteins ....
الإتاحة: https://doi.org/10.1093/humrep/deab230Test
https://research.vumc.nl/en/publications/53d6464d-d112-4a54-b629-4c956d3f0bf3Test
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85123388818&origin=inwardTest
https://www.ncbi.nlm.nih.gov/pubmed/34755185Test -
55دورية أكاديمية
المؤلفون: Sluijs, P.J. van der, Alders, M., Dingemans, A.J.M., Parbhoo, Kareesma, Bon, B.W. van, Dempsey, J.C., Vries, B.B.A. de, Maystadt, I., Santen, G.W.E.
المصدر: Genes, 12, 8
مصطلحات موضوعية: All institutes and research themes of the Radboud University Medical Center, Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience
العلاقة: https://repository.ubn.ru.nl//bitstream/handle/2066/237017/237017.pdfTest; https://repository.ubn.ru.nl/handle/2066/237017Test; https://doi.org/10.3390/genes12081275Test
الإتاحة: https://doi.org/10.3390/genes12081275Test
https://repository.ubn.ru.nl//bitstream/handle/2066/237017/237017.pdfTest
https://repository.ubn.ru.nl/handle/2066/237017Test -
56دورية أكاديمية
المؤلفون: Levy, M.A., Beck, D.B., Metcalfe, K., Douzgou, S., Sithambaram, S., Cottrell, T., Ansar, M., Kerkhof, J., Mignot, C., Nougues, M.C., Keren, B., Moore, H.W., Oegema, R., Giltay, J.C., Simon, M., Jaarsveld, R.H. van, Bos, J., Haelst, M. van, Motazacker, M.M., Boon, E.M.J., Santen, G.W.E., Ruivenkamp, C.A.L., Alders, M., Luperchio, T.R., Boukas, L., Ramsey, K., Narayanan, V., Schaefer, G.B., Bonasio, R., Doheny, K.F., Stevenson, R.E., Banka, S., Sadikovic, B., Fahrner, J.A.
المصدر: npj Genomic Medicine
العلاقة: lumc-id: 122248876; https://hdl.handle.net/1887/3256845Test
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57دورية أكاديمية
المؤلفون: Shows, TB, Alders, M, Bennett, S, Burbee, D, Cartwright, P, Chandrasekharappa, S, Cooper, P, Courseaux, A, Davies, C, Devignes, MD, Devilee, P, Elliott, R, Evans, G, Fantes, J, Garner, H, Gaudray, P, Gerhard, DS, Gessler, M, Higgins, M, Hummerich, H, James, M, Lagercrantz, J, Litt, M, Little, P, Mannens, M, Munroe, D, Nowak, N, OBrien, S, Parker, N, Perlin, M, Reid, L, Richard, C, Sawicki, M, Swallow, D, Thakker, R, vanHeyningen, V, vanSchothorst, E, Vorechovsky, I, Wadelius, C, Weber, B, Zabel, B
المصدر: CYTOGENETICS AND CELL GENETICS. 74(1-2):2-52
مصطلحات موضوعية: Medicin och hälsovetenskap
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58دورية أكاديمية
المؤلفون: van Spaendonck-Zwarts, K. Y., Posafalvi, A., van den Berg, M. P., Hilfiker-Kleiner, D., Bollen, I. A. E., Sliwa, K., Alders, M., Almomani, R., van Langen, I. M., van der Meer, P., Sinke, R. J., van der Velden, J., Van Veldhuisen, D. J., van Tintelen, J. P., Jongbloed, J. D. H.
المصدر: European Heart Journal ; volume 35, issue 32, page 2165-2173 ; ISSN 0195-668X 1522-9645
الإتاحة: https://doi.org/10.1093/eurheartj/ehu050Test
http://academic.oup.com/eurheartj/article-pdf/35/32/2165/17354528/ehu050.pdfTest -
59دورية أكاديمية
المؤلفون: Nolte, J.W., Alders, M., Karssemakers, L.H.E., Becking, A.G., Hennekam, R.C.M.
المصدر: Nolte , J W , Alders , M , Karssemakers , L H E , Becking , A G & Hennekam , R C M 2020 , ' Unilateral condylar hyperplasia in hemifacial hyperplasia, is there genetic proof of overgrowth? ' , International Journal of Oral and Maxillofacial Surgery , vol. 49 , no. 11 , pp. 1464-1469 . https://doi.org/10.1016/j.ijom.2020.02.002Test
مصطلحات موضوعية: /dk/atira/pure/sustainabledevelopmentgoals/clean_water_and_sanitation, name=SDG 6 - Clean Water and Sanitation
الإتاحة: https://doi.org/10.1016/j.ijom.2020.02.002Test
https://research.vu.nl/en/publications/6f7c727f-f399-4521-b99c-e706c9d391b7Test
https://hdl.handle.net/1871.1/6f7c727f-f399-4521-b99c-e706c9d391b7Test -
60دورية أكاديمية
المؤلفون: Nolte, J.W., Alders, M., Karssemakers, L.H.E., Becking, A.G., Hennekam, R.C.M.
المصدر: Nolte , J W , Alders , M , Karssemakers , L H E , Becking , A G & Hennekam , R C M 2020 , ' Molecular basis of unilateral condylar hyperplasia? ' , International Journal of Oral and Maxillofacial Surgery , vol. 49 , no. 11 , pp. 1397-1401 . https://doi.org/10.1016/j.ijom.2020.01.017Test
مصطلحات موضوعية: /dk/atira/pure/sustainabledevelopmentgoals/clean_water_and_sanitation, name=SDG 6 - Clean Water and Sanitation
الإتاحة: https://doi.org/10.1016/j.ijom.2020.01.017Test
https://research.vu.nl/en/publications/039a4cd1-f8ee-469e-9260-f0c523e7a857Test
https://hdl.handle.net/1871.1/039a4cd1-f8ee-469e-9260-f0c523e7a857Test
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