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1دورية أكاديمية
المؤلفون: Modenato, C., Kumar, K., Moreau, C., Martin-Brevet, S., Huguet, G., Schramm, C., Jean-Louis, M., Martin, C.-O., Younis, N., Tamer, P., Douard, E., Thébault-Dagher, F., Côté, V., Charlebois, A.-R., Deguire, F., Maillard, A.M., Rodriguez-Herreros, B., Pain, A., Richetin, S., Addor, M.-C., Andrieux, J., Arveiler, B., Baujat, G., Sloan-Béna, F., Belfiore, M., Bonneau, D., Bouquillon, S., Boute, O., Brusco, A., Busa, T., CABERG, Jean-Hubert, Campion, D., Colombert, V., Cordier, M.-P., David, A., Debray, François-Guillaume, Delrue, M.-A., Doco-Fenzy, M., Dunkhase-Heinl, U., Edery, P., Fagerberg, C., Faivre, L., Forzano, F., Genevieve, D., Gérard, M., Giachino, D., Guichet, A., Guillin, O., Héron, D., Isidor, B., Jacquette, A., Jaillard, S., Journel, H., Keren, B., Lacombe, D., Lebon, S., Le Caignec, C., Lemaître, M.-P., Lespinasse, J., Mathieu-Dramart, M., Mercier, S., Mignot, C., Missirian, C., Petit, F., Pilekær Sørensen, K., Pinson, L., Plessis, G., Prieur, F., Raymond, A., Rooryck-Thambo, C., Rossi, M., Sanlaville, D., Schlott Kristiansen, B., Schluth-Bolard, C., Till, M., Van Haelst, M., Van Maldergem, L., Alupay, H., Aaronson, B., Ackerman, S., Ankenman, K., Anwar, A., Atwell, C., Bowe, A., Beaudet, A.L., Benedetti, M., Berg, J., Berman, J., Berry, L.N., Bibb, A.L., Blaskey, L., Brennan, J., Brewton, C.M., Buckner, R., Bukshpun, P., Burko, J., Cali, P., Cerban, B., Chang, Y., Cheong, M., Chow, V., Chu, Z., Chudnovskaya, D., Cornew, L., Dale, C., Dell, J., Dempsey, A.G., Deschamps, T., Earl, R., Edgar, J., Elgin, J., Olson, J.E., Evans, Y.L., Findlay, A., Fischbach, G.D., Fisk, C., Fregeau, B., Gaetz, B., Gaetz, L., Garza, S., Gerdts, J., Glenn, O., Gobuty, S.E., Golembski, R., Greenup, M., Heiken, K., Hines, K., Hinkley, L., Jackson, F.I., Jenkins, J., Jeremy, R.J., Johnson, K., Kanne, S.M., Kessler, S., Khan, S.Y., Ku, M., Kuschner, E., Laakman, A.L., Lam, P., Lasala, M.W., Lee, H., LaGuerre, K., Levy, S., Cavanagh, A.L., Llorens, A.V., Campe, K.L., Luks, T.L., Marco, E.J., Martin, S., Martin, A.J., Marzano, G., Masson, C., McGovern, K.E., Keehn, R.M.N., Miller, D.T., Miller, F.K., Moss, T.J., Murray, R., Nagarajan, S.S., Nowell, K.P., Owen, J., Paal, A.M., Packer, A., Page, P.Z., Paul, B.M., Peters, A., Peterson, D., Poduri, A., Pojman, N.J., Porche, K., Proud, M.B., Qasmieh, S., Ramocki, M.B., Reilly, B., Roberts, T.P.L., Shaw, D., Sinha, T., Smith-Packard, B., Gallagher, A.S., Swarnakar, V., Thieu, T., Triantafallou, C., Vaughan, R., Wakahiro, M., Wallace, A., Ward, T., Wenegrat, J., Wolken, A., Melie-Garcia, L., Kushan, L., Silva, A.I., van den Bree, M.B.M., Linden, D.E.J., Owen, M.J., Hall, J., Lippé, S., Chakravarty, M., Bzdok, D., Montreal Neurological Institute, McGill University, Bearden, C.E., Draganski, B., Jacquemont, S., 16p11.2 European Consortium, Simons Searchlight Consortium
المصدر: Translational Psychiatry, 11 (1) (2021)
مصطلحات موضوعية: Life sciences, Genetics & genetic processes, Sciences du vivant, Génétique & processus génétiques
Relation: urn:issn:2158-3188
URL الوصول: https://orbi.uliege.be/handle/2268/297321
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المؤلفون: Olde Keizer, Richelle A.C.M., Marouane, Abderrahim, Kerstjens-Frederikse, Wilhelmina S., Deden, A. Chantal, Lichtenbelt, Klaske D., Jonckers, Tinneke, Vervoorn, Marieke, Vreeburg, M., Henneman, Lidewij, de Vries, Linda S., Sinke, Richard J., Pfundt, Rolph, Stevens, Servi J.C., Andriessen, Peter, van Lingen, Richard A., Nelen, Marcel, Scheffer, Hans, Stemkens, Daphne, Oosterwijk, Cor, van Amstel, Hans Kristian Ploos, de Boode, W. P., van Zelst-Stams, W., Frederix, Geert W.J., Vissers, L. E.L.M., Henneman, L., van Haelst, M. M., Sistermans, E. A., Cornel, M. C., Misra-Isrie, M., Mannens, M. M.A.M., Waisfisz, Q., van Hagen, J. M., Brooks, A. S., Barakat, T. S., Hoefsloot, E. H., van Lingen, R. A., Ruivenkamp, C. A.L., Koene, S., Rutten, J. W., de Koning, B., Stevens, S. J.C., van den Wijngaard, A., Stegmann, A. P.A., Deden, A. C., Rodenburg, W., Sinke, R. J., van der Velde, K. J., de Vries, L. S., Frederix, G. W.J., Oegema, R.
المساهمون: Clinical Genetics, Pediatric Surgery, Radiology & Nuclear Medicine, Internal Medicine, Department of Finance, Cell biology, Cardiothoracic Surgery, Molecular Genetics, Pathology, Erasmus School of Law, Health Economics (HE)
المصدر: European Journal of Pediatrics. Springer-Verlag
وصف الملف: application/pdf
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3دورية أكاديمية
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المؤلفون: Van Schaik, J., Welling, M., De Groot, C., Abawi, O., Burghard, M., Kleinendorst, L., Van der Voorn, B., Van Haelst, M., Ophuis, B. Oude, Bakker, B., Tissing, W., Kamp, G., Rotteveel, J., Schouten-Van Meeteren, A., Van de Akker, E., Van Santen, H.
المساهمون: Obstetrics and gynaecology, Amsterdam Reproduction & Development, Clinical genetics, Intensive care medicine, Pediatrics, Amsterdam Neuroscience - Complex Trait Genetics
المصدر: Pediatric Blood and Cancer, 68, S292-S293. Wiley-Liss Inc.
Van Schaik, J, Welling, M, De Groot, C, Abawi, O, Burghard, M, Kleinendorst, L, Van der Voorn, B, Van Haelst, M, Ophuis, B O, Bakker, B, Tissing, W, Kamp, G, Rotteveel, J, Schouten-Van Meeteren, A, Van de Akker, E & Van Santen, H 2021, ' Dextro-Amphetamine Treatment for Hypothalamic Obesity in Children Surviving Brain Tumors or Other Causes ', Pediatric Blood and Cancer, vol. 68, pp. S292-S293 . -
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المؤلفون: Lehalle, D., Vabres, P., Bierhals, T., Cho, M. T., Cogne, B., Avila, M., Carmignac, V., Duplomb-Jego, L., De Bont, E., Duffourd, Y., Duijkers, F., Elpeleg, O., Fattal-Valevski, A., Genevieve, D., Guimier, A., Harris, D., Hempel, M., Isidor, B., Jouan, T., Kuentz, P., Lichtenbelt, K., Ramey, V. Loik, Pasquier, L., St-Onge, J., Sorlin, A., Thevenon, J., Torti, E., Van Gassen, K., Van Haelst, M., van Koningsbruggen, S., Riviere, J., Thauvin, C., Betschinger, J., Faivre, L.
المساهمون: Clinical genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development
المصدر: Lehalle, D, Vabres, P, Bierhals, T, Cho, M T, Cogne, B, Avila, M, Carmignac, V, Duplomb-Jego, L, De Bont, E, Duffourd, Y, Duijkers, F, Elpeleg, O, Fattal-Valevski, A, Genevieve, D, Guimier, A, Harris, D, Hempel, M, Isidor, B, Jouan, T, Kuentz, P, Lichtenbelt, K, Ramey, V L, Pasquier, L, St-Onge, J, Sorlin, A, Thevenon, J, Torti, E, Van Gassen, K, Van Haelst, M, van Koningsbruggen, S, Riviere, J, Thauvin, C, Betschinger, J & Faivre, L 2019, ' De novo missense mutations in the X-linked TFE3 gene cause intellectual disability with pigmentary mosaicism and storage disorder-like features ', European Journal of Human Genetics, vol. 27, pp. 1094-1094 .
European Journal of Human Genetics, 27, 1094-1094. Nature Publishing Group -
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المصدر: Tijdschrift voor kindergeneeskunde. October 2001 69(5):63-66
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8دورية أكاديمية
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المؤلفون: Kleinendorst, L., Abawi, O., Brandsma, A. E., Jongejan, M. H., Van Rossum, E. F. C., Van der Zwaag, B., Van den Akker, E. L. T., Van Haelst, M. M.
المساهمون: Clinical genetics, General practice, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development
المصدر: Kleinendorst, L, Abawi, O, Brandsma, A E, Jongejan, M H, Van Rossum, E F C, Van der Zwaag, B, Van den Akker, E L T & Van Haelst, M M 2019, ' Genetic causes of early onset obesity are frequently identified in a tertiary pediatric obesity cohort ', European Journal of Human Genetics, vol. 27, pp. 86-87 .
European Journal of Human Genetics, 27, 86-87. Nature Publishing Group -
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المؤلفون: Kleinendorst, L, van Haelst, M, van den Akker, Erica
المساهمون: Pediatrics
مصطلحات موضوعية: SDG 3 - Good Health and Well-being
URL الوصول: https://explore.openaire.eu/search/publication?articleId=narcis______::dd6e815699acd4d9cfd1fa6bcd3457d9
https://pure.eur.nl/en/publications/b84736f0-9882-47a0-afd8-be2dbfa05473
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