المؤلفون: Fiona Macdonald, Colin E. Willoughby, E Forsythe, Gudrun E. Moore, Marielle Alders, Derek Lim, Jan Maarten Cobben, S Abu Amero, Emma Wakeling, Rebecca L. Poole, Deborah J G Mackay, Sandeep Kumar, Eamonn R. Maher, M. M. van Haelst, I K Temple, Cls Turner, T Tangeraas, SM Price, Jet Bliek

المساهمون: ACS - Amsterdam Cardiovascular Sciences, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Other Research, Human Genetics, ANS - Amsterdam Neuroscience, Paediatric Genetics, Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D), Pediatric surgery

المصدر: Journal of medical genetics, 47(11), 760-768. BMJ Publishing Group
JOURNAL OF MEDICAL GENETICS, 47(11), 760-768. BMJ PUBLISHING GROUP
Wakeling, E L, Amero, S A, 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 M 2010, ' Epigenotype-phenotype correlations in Silver-Russell syndrome ', Journal of Medical Genetics, vol. 47, no. 11, pp. 760-8 . https://doi.org/10.1136/jmg.2010.079111
Journal of Medical Genetics
Journal of Medical Genetics, 47(11), 760-8. BMJ Publishing Group

مصطلحات موضوعية: Male, Pediatrics, RNA, Untranslated, Movement disorders, mUPD7, HYPOMETHYLATION, 11p15 hypomethylation, Intrauterine growth restriction, PHENOTYPE, Epigenesis, Genetic, Prospective Studies, Child, Prospective cohort study, Genetics (clinical), Chromosome 7 (human), Genetics, education.field_of_study, Silver Russell syndrome, CHROMOSOME 11P15, METHYLATION, Uniparental disomy, Potassium Channels, Voltage-Gated, Child, Preschool, IMPRINTING CENTER REGION, Medical genetics, Female, RNA, Long Noncoding, Original Article, imprinting, medicine.symptom, MATERNAL UNIPARENTAL DISOMY, Chromosomes, Human, Pair 7, Adult, medicine.medical_specialty, Adolescent, DYSTONIA, Population, Biology, Genomic Imprinting, Young Adult, ASSISTED REPRODUCTIVE TECHNOLOGY, medicine, Humans, education, Genetic Association Studies, SPECTRUM, Chromosomes, Human, Pair 11, Silver–Russell syndrome, Infant, DNA Methylation, Uniparental Disomy, medicine.disease, Silver-Russell Syndrome, clinical genetics, GROWTH-RETARDATION

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd22e69e1b1d8631e86af562af8e4fd5
https://doi.org/10.1136/jmg.2010.079111

المؤلفون: J.-M. Elalouf, J.R. Mann, S.C. Barton, A.S. Garfield, C. Rasberry, K. Okumura, M.S. Gross, T. Yokomine, Barbara Hutter, C.M. Williamson, A. Ogura, Timothy Bestor, M. Kimura, C. Gallou-Kabani, S. Khosla, G. Cathala, C. Jacquet, P. Stanier, Y. Hayashizaki, H. Soejima, P. Hajkova, J.P. Jais, W. Mills, A. Ward, C. Junien, F. Ishino, R. Ono, N. Wake, C. Ciaudo, G. Mendiratta, J.R. Chaillet, S. Abu-Amero, N. Maeda, T.H. Vu, A. Fabre, L. Estabrooks, L. Steele, C. Shuman, R. Nasser, Y. Sekita, H. Seitz, Colin V. Beechey, M. Irie, Kenichiro Hata, A.C. Smith, M. Tsudzuki, T. Ochiya, T. Kaneko-Ishino, David Monk, Paul D. Soloway, T. Rubin, M.-L. Bortolin, I. Hatada, B. Horsthemke, A. Gossler, N. Miyoshi, R.L. Jirtle, L. Dandolo, N. Aptel, T. Ohhata, M. Tevendale, A. Paoloni-Giacobino, T. Ito, H. Sasaki, B. Cattanach, T. Saito, Yuko Hoki, L. Milligan, D. Haig, B. Tycko, Anne C. Ferguson-Smith, M. Yokoyama, T. Mukai, Takashi Sado, Gavin Kelsey, P.A. Latos, L. Han, T. Forné, A.S. Aylsworth, P.E. Szabó, M.A. Surani, T. Kono, L. Zakin, Jörn Walter, T. Abe, J. Hyo-Jung, G.E. Moore, A. Bourdet, M. Fukasawa, K. Buiting, B.M. Cattanach, Takahiro Arima, M. Spielman, K. Okamura, A. Vigé, J. Cavaillé, T. Kishino, R. Shemer, Tarang Khare, K. Regha, A. Razin, W. Reik, M. Watkins, Robert Feil, K. Higashimoto, E. Heard, A.R. Hoffman, K. Schuster-Gossler, M.T. McDonald, T. Horii, S. Kobayashi, I. Okamoto, Gary F. Moore, R.A. Drewell, Marisa S. Bartolomei, Michael Weber, S. Apostolidou, H. Kobayashi, F.M. Smith, C. Rusniok, M.-A. Ripoche, M. Kaneda, R. Weksberg, S. Morita, H. Wagatsuma, Thomas A. Moore, A. Plagge, P.N. Ray, T. Ikemura, Jo Peters, V. Brahmachari, P. Avner, K.J. Reese, H. Hagège, H. Royo, J. Weissenbach, J. Matsuda, L. Spahn, D. Solter, R.J. Scott, Martina Paulsen, B. Kantor, Y. Kohara, Déborah Bourc'his, C. Suda, A. Gabory, Rebecca J. Holmes, A. Lewis, T. Kohda, Alexandre Wagschal, T. Yoshimizu

المصدر: Cytogenetic and Genome Research. 113:351-352

مصطلحات موضوعية: Botany, Genetics, Zoology, Biology, Molecular Biology, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::88681cc1ff9e0d666b54a4a4f3ee5c48
https://doi.org/10.1159/000092443

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