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1دورية أكاديمية
المؤلفون: Curic, E, Ewans, L, Pysar, R, Taylan, F, Botto, LD, Nordgren, A, Gahl, W, Palmer, EE
المصدر: Orphanet journal of rare diseases. 18(1):348
مصطلحات موضوعية: Medicin och hälsovetenskap
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2دورية أكاديمية
المؤلفون: Smol, T.Aff1, Aff2, Petit, F.Aff2, Aff3, Piton, A., Keren, B., Sanlaville, D., Afenjar, A., Baker, S., Bedoukian, E. C., Bhoj, E. J., Bonneau, D., Boudry-Labis, E., Bouquillon, S., Boute-Benejean, O.Aff2, Aff3, Caumes, R., Chatron, N., Colson, C.Aff2, Aff3, Coubes, C., Coutton, C., Devillard, F., Dieux-Coeslier, A.Aff2, Aff3, Doco-Fenzy, M., Ewans, L. J., Faivre, L.Aff15, Aff16, Fassi, E., Field, M., Fournier, C., Francannet, C., Genevieve, D., Giurgea, I., Goldenberg, A., Green, A. K., Guerrot, A. M., Heron, D., Isidor, B., Keena, B. A., Krock, B. L., Kuentz, P., Lapi, E., Le Meur, N., Lesca, G., Li, D., Marey, I., Mignot, C., Nava, C., Nesbitt, A., Nicolas, G., Roche-Lestienne, C., Roscioli, T., Satre, V., Santani, A., Stefanova, M., Steinwall Larsen, S., Saugier-Veber, P., Picker-Minh, S., Thuillier, C., Verloes, A., Vieville, G., Wenzel, M., Willems, M., Whalen, S., Zarate, Y. A., Ziegler, A., Manouvrier-Hanu, S.Aff2, Aff3, Kalscheuer, V. M., Gerard, B., Ghoumid, JamalAff2, Aff3
المصدر: neurogenetics. 19(2):93-103
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3دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
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4دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
5مورد إلكتروني
المؤلفون: Cheng, H, Capponi, S, Wakeling, E, Marchi, E, Li, Q, Zhao, M, Weng, C, Stefan, PG, Ahlfors, H, Kleyner, R, Rope, A, Lumaka, A, Lukusa, P, Devriendt, K, Vermeesch, J, Posey, JE, Palmer, EE, Murray, L, Leon, E, Diaz, J, Worgan, L, Mallawaarachchi, A, Vogt, J, de Munnik, SA, Dreyer, L, Baynam, G, Ewans, L, Stark, Z, Lunke, S, Gonçalves, AR, Soares, G, Oliveira, J, Fassi, E, Willing, M, Waugh, JL, Faivre, L, Riviere, JB, Moutton, S, Mohammed, S, Payne, K, Walsh, L, Begtrup, A, Guillen Sacoto, MJ, Douglas, G, Alexander, N, Buckley, MF, Mark, PR, Adès, LC, Sandaradura, SA, Lupski, JR, Roscioli, T, Agrawal, PB, Kline, AD, Wang, K, Timmers, HTM, Lyon, GJ
مصطلحات الفهرس: 0604 Genetics, 1103 Clinical Sciences, text, Journal Article, Journal Article
URL:
http://handle.unsw.edu.au/1959.4/unsworks_62386 https://orcid.org/0000-0003-1844-215X https://orcid.org/0000-0003-1844-215X
Human Mutation, 41, 2, 449-464 -
6مورد إلكتروني
المؤلفون: Wilson M., Cliffe C., Elakis G., Zhu Y., Nixon C., Smith J., Turner A., Walsh M., Wallis M., Roscioli T., Worgan L., Schofield D., Lau C., Kirk E., Mead S., Buckley M., Hunter M., Fahey M., Mullan G., Lang S., Richards A., Quayum N., Ades L., Amor D., Bakshi M., Berman Y., Brown N., Chung C., Colley A., Collins F., Edwards M., Ellaway C., Ewans L., Field M., Freckmann M., Gabbett M., Goel H., Ghedia S., Goodwin L., Hackett A., Jones K., Josephi-Taylor S., Kamian B., Kennedy D., Ma A., McGillivray G., Mowat D., Palmer E., Pinner J., Rajagopalan S., Ronan A., Sachdev R., Sandaradura S., Sinnerbrink I.
مصطلحات الفهرس: patient referral, adult, bioinformatics, cost effectiveness analysis, drug safety, female, human, library, major clinical study, moyamoya disease, patient safety, pipeline, practice guideline, pregnancy, prenatal diagnosis, recurrence risk, whole exome sequencing, proton, conference abstract, Conference Abstract
URL:
https://repository.monashhealth.org/monashhealthjspui/handle/1/36513
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7مورد إلكتروني
المؤلفون: Cheng, H., Capponi, S., Wakeling, E., Marchi, E., Li, Q., Zhao, M., Weng, C., Stefan, P.G., Ahlfors, H., Kleyner, R., Rope, A., Lumaka, A., Lukusa, P., Devriendt, K., Vermeesch, J., Posey, J.E., Palmer, E.E., Murray, L., Leon, E., Diaz, J., Worgan, L., Mallawaarachchi, A., Vogt, J., Munnik, S.A., Dreyer, L., Baynam, G., Ewans, L., Stark, Z., Lunke, S., Gonçalves, A.R., Soares, G., Oliveira, J., Fassi, E., Willing, M., Waugh, J.L., Faivre, L., Riviere, J‐B, Moutton, S., Mohammed, S., Payne, K., Walsh, L., Begtrup, A., Guillen Sacoto, M.J., Douglas, G., Alexander, N., Buckley, M.F., Mark, P.R., Adès, L.C., Sandaradura, S.A., Lupski, J.R., Roscioli, T., Agrawal, P.B., Kline, A.D., Wang, K., Timmers, H.T.M., Lyon, G.J.
المصدر: Cheng, H., Capponi, S., Wakeling, E., Marchi, E., Li, Q., Zhao, M., Weng, C., Stefan, P.G., Ahlfors, H., Kleyner, R., Rope, A., Lumaka, A., Lukusa, P., Devriendt, K., Vermeesch, J., Posey, J.E., Palmer, E.E., Murray, L., Leon, E., Diaz, J., Worgan, L., Mallawaarachchi, A., Vogt, J., Munnik, S.A., Dreyer, L., Baynam, G. <
مصطلحات الفهرس: Journal Article
URL:
https://researchrepository.murdoch.edu.au/id/eprint/53466/ https://researchrepository.murdoch.edu.au/id/eprint/53466
full_text_status:none -
8مورد إلكتروني
المؤلفون: Cheng, H, Capponi, S, Wakeling, E, Marchi, E, Li, Q, Zhao, M, Weng, C, Stefan, PG, Ahlfors, H, Kleyner, R, Rope, A, Lumaka, A, Lukusa, P, Devriendt, K, Vermeesch, J, Posey, JE, Palmer, EE, Murray, L, Leon, E, Diaz, J, Worgan, L, Mallawaarachchi, A, Vogt, J, de Munnik, SA, Dreyer, L, Baynam, G, Ewans, L, Stark, Z, Lunke, S, Goncalves, AR, Soares, G, Oliveira, J, Fassi, E, Willing, M, Waugh, JL, Faivre, L, Riviere, J-B, Moutton, S, Mohammed, S, Payne, K, Walsh, L, Begtrup, A, Sacoto, MJG, Douglas, G, Alexander, N, Buckley, MF, Mark, PR, Ades, LC, Sandaradura, SA, Lupski, JR, Roscioli, T, Agrawal, PB, Kline, AD, Wang, K, Timmers, HTM, Lyon, GJ
مصطلحات الفهرس: Journal Article
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9مورد إلكتروني
المؤلفون: Poulton, C., Azmanov, D., Atkinson, V., Beilby, J., Ewans, L., Gration, D., Dreyer, L., Shetty, V., Peake, C., McCormack, E., Palmer, Richard, Lewis, B., Dawkins, H., Broley, S., Baynam, G.
مصطلحات الفهرس: Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, Aboriginal, IGF2, macrocephaly, Silver-Russel syndrome, IGF2 MUTATION, Journal Article
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10مورد إلكتروني
المؤلفون: Ohnesorg, T, van den Bergen, JA, Belluoccio, D, Shankara-Narayana, N, Kean, A-M, Vasilaras, A, Ewans, L, Ayers, KL, Sinclair, AH
مصطلحات الفهرس: Journal Article