نتائج البحث - Sayeda Abu‐Amero

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  1. 1
    The genetic aetiology of Silver-Russell syndrome

    The genetic aetiology of Silver-Russell syndrome حسب Sayeda Abu‐Amero, David Monk, Jennifer M. Frost, Michael Preece, Philip Stanier, Gudrun E. Moore

    منشور في 2007
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  2. 2
    The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta

    The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta حسب M. Noguer-Dance, Sayeda Abu‐Amero, Mohamed Al-Khtib, A. Lefèvre, P. Coullin, Gudrun E. Moore, Jérôme Cavaillé

    منشور في 2010
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  3. 3
    Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome

    Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome حسب David Monk, Emma Wakeling, Virginia K. Proud, Megan P. Hitchins, Sayeda Abu‐Amero, Philip Stanier, Michael A. Preece, Gudrun E. Moore

    منشور في 2000
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  4. 4
    High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta

    High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta حسب Caroline Daelemans, Matthew E. Ritchie, Guillaume Smits, Sayeda Abu‐Amero, Ian Sudbery, Matthew S. Forrest, Susana Campino, Taane G. Clark, Philip Stanier, Dominic Kwiatkowski, Panos Deloukas, Emmanouil T. Dermitzakis, Simon Tavaré, Gudrun E. Moore, Ian Dunham

    منشور في 2010
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  5. 5
    Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development

    Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development حسب Veronica A. Kinsler, Sayeda Abu‐Amero, Peter S. Budd, Ian J. Jackson, Susan M. Ring, Kate Northstone, David J. Atherton, Neil Bulstrode, Philip Stanier, Raoul C. M. Hennekam, Neil J. Sebire, Gudrun E. Moore, Eugene Healy

    منشور في 2012
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  6. 6
    Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution

    Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution حسب Layla Parker-Katiraee, Andrew R. Carson, Takahiro Yamada, Philippe Arnaúd, Robert Feil, Sayeda Abu‐Amero, Gudrun E Moore, Masahiro Kaneda, George H. Perry, Anne C. Stone, Charles Lee, Makiko Meguro‐Horike, Hiroyuki Sasaki, Keiko Kobayashi, Kazuhiko Nakabayashi, Stephen W. Scherer

    منشور في 2007
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  7. 7
    Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

    Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS حسب Veronica A. Kinsler, Anna Thomas, Miho Ishida, Neil Bulstrode, Sam Loughlin, Sandra Hing, Jane Chalker, Kathryn J. McKenzie, Sayeda Abu‐Amero, Olga Slater, Estelle Chanudet, Rodger Palmer, Deborah Morrogh, Philip Stanier, Eugene Healy, Neil J. Sebire, Gudrun E. Moore

    منشور في 2013
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  8. 8
    Trans effects of chromosome aneuploidies on DNA methylation patterns in human Down syndrome and mouse models

    Trans effects of chromosome aneuploidies on DNA methylation patterns in human Down syndrome and mouse models حسب Maite Mendióroz, Catherine Do, Xiaoling Jiang, Chunhong Liu, Huferesh K. Darbary, Charles F. Lang, J. P. Lin, Anna Thomas, Sayeda Abu‐Amero, Philip Stanier, Alexis M. Temkin, Alexander Yale, Meng-Min Liu, Yang Li, Martha Salas, Kristi Kerkel, George T. Capone, Wayne Silverman, Yichao Yu, Gudrun E. Moore, Jerzy Węgiel, Benjamin Tycko

    منشور في 2015
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  9. 9
    The role and interaction of imprinted genes in human fetal growth

    The role and interaction of imprinted genes in human fetal growth حسب Gudrun E. Moore, Miho Ishida, Charalambos Demetriou, Lara Al-Olabi, Lydia J. Leon, Anna Thomas, Sayeda Abu‐Amero, Jennifer M. Frost, Jaime L. Stafford, Chaoqun Yao, Andrew Duncan, Rachel Baigel, Marina Brimioulle, Isabel Iglesias‐Platas, Sophia Apostolidou, Reena Aggarwal, John C. Whittaker, Argyro Syngelaki, K. H. Nicolaides, Lesley Regan, David Monk, Philip Stanier

    منشور في 2015
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  10. 10
    Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer

    Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer حسب Yoko Itō, Thibaud Koessler, Ashraf E.K. Ibrahim, Sushma Rai, Sarah L. Vowler, Sayeda Abu‐Amero, Ana-Luisa Silva, Ana-Teresa Maia, Joanna E. Huddleston, Santiago Uribe‐Lewis, Kathryn Woodfine, Maja Jagodic, Raffaella Nativio, Alison M. Dunning, Gudrun E. Moore, Elena Klenova, Sheila Bingham, Paul D.P. Pharoah, James D. Brenton, Stephan Beck, Manjinder S. Sandhu, Adele Murrell

    منشور في 2008
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  11. 11
    Genetic analyses in small-for-gestational-age newborns

    Genetic analyses in small-for-gestational-age newborns حسب Stalman SE, Nita Solanky, M Ishida, Cristina Alemán-Charlet, Sayeda Abu‐Amero, Mariëlle Alders, Lucas Alvizi, William Baird, Charalambos Demetriou, Peter Henneman, Catherine James, Knegt LC, Leon LJ, Mannens Mmam, Mul AN, Nibbering NA, Emma Peskett, Rezwan FI, Carrie Ris‐Stalpers, van der Post JAM, Kamp Ga, Plötz Fb, Wit Jm, Philip Stanier, Moore Ge, Hennekam Rc

    منشور في 2018
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  12. 12
    Genetic Analyses in Small-for-Gestational-Age Newborns

    Genetic Analyses in Small-for-Gestational-Age Newborns حسب Susanne E. Stalman, Nita Solanky, Miho Ishida, Cristina Alemán-Charlet, Sayeda Abu‐Amero, Mariëlle Alders, Lucas Alvizi, William Baird, Charalambos Demetriou, Peter Henneman, Chela James, Lia Knegt, Lydia J. Leon, Marcel M.A.M. Mannens, Adi N Mul, Nicole A Nibbering, Emma Peskett, Faisal I. Rezwan, Carrie Ris‐Stalpers, Joris van der Post, Gerdine A. Kamp, Frans B. Plötz, Jan M. Wit, Philip Stanier, Gudrun E. Moore, Raoul C. M. Hennekam

    منشور في 2018
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