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Material Type: Artigo
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Phenotype of genetically confirmed Silver-Russell syndrome beyond childhoodLokulo-Sodipe, Oluwakemi ; Ballard, Lisa ; Child, Jenny ; Inskip, Hazel M ; Byrne, Christopher D ; Ishida, Miho ; Moore, Gudrun E ; Wakeling, Emma L ; Fenwick, Angela ; Mackay, Deborah J G ; Davies, Justin Huw ; Temple, I KarenJournal of medical genetics, 2020-10, Vol.57 (10), p.683-691 [Periódico revisado por pares]England: BMJ Publishing Group LTDTexto completo disponível |
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Material Type: Artigo
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Epigenotype–phenotype correlations in Silver–Russell syndromeWakeling, E L ; Amero, S Abu ; Alders, M ; Bliek, J ; Forsythe, E ; Kumar, S ; Lim, D H ; MacDonald, F ; Mackay, D J ; Maher, E R ; Moore, G E ; Poole, R L ; Price, S M ; Tangeraas, T ; Turner, C L S ; Van Haelst, M M ; Willoughby, C ; Temple, I K ; Cobben, J MJournal of medical genetics, 2010-11, Vol.47 (11), p.760-768 [Periódico revisado por pares]London: BMJ Publishing Group LtdTexto completo disponível |
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3 |
Material Type: Artigo
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Effectiveness of continuous glucose monitoring in pregnant women with diabetes: randomised clinical trialMurphy, Helen R ; Rayman, Gerry ; Lewis, Karen ; Kelly, Susan ; Johal, Balroop ; Duffield, Katherine ; Fowler, Duncan ; Campbell, Peter J ; Temple, Rosemary CBMJ, 2008-10, Vol.337 (7675), p.907-910 [Periódico revisado por pares]England: British Medical Journal Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspringBegemann, Matthias ; Rezwan, Faisal I ; Beygo, Jasmin ; Docherty, Louise E ; Kolarova, Julia ; Schroeder, Christopher ; Buiting, Karin ; Chokkalingam, Kamal ; Degenhardt, Franziska ; Wakeling, Emma L ; Kleinle, Stephanie ; González Fassrainer, Daniela ; Oehl-Jaschkowitz, Barbara ; Turner, Claire L S ; Patalan, Michal ; Gizewska, Maria ; Binder, Gerhard ; Bich Ngoc, Can Thi ; Chi Dung, Vu ; Mehta, Sarju G ; Baynam, Gareth ; Hamilton-Shield, Julian P ; Aljareh, Sara ; Lokulo-Sodipe, Oluwakemi ; Horton, Rachel ; Siebert, Reiner ; Elbracht, Miriam ; Temple, Isabel Karen ; Eggermann, Thomas ; Mackay, Deborah J GJournal of medical genetics, 2018-07, Vol.55 (7), p.497-504 [Periódico revisado por pares]England: BMJ Publishing Group LTDTexto completo disponível |
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5 |
Material Type: Artigo
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Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genesDocherty, Louise E ; Rezwan, Faisal I ; Poole, Rebecca L ; Jagoe, Hannah ; Lake, Hannah ; Lockett, Gabrielle A ; Arshad, Hasan ; Wilson, David I ; Holloway, John W ; Temple, I Karen ; Mackay, Deborah J GJournal of medical genetics, 2014-04, Vol.51 (4), p.229-238 [Periódico revisado por pares]England: BMJ Publishing Group LTDTexto completo disponível |