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1دورية أكاديمية
المؤلفون: Sansbury, Francis H, Kirel, Birgül, Caswell, Richard, Lango Allen, Hana, Flanagan, Sarah E, Hattersley, Andrew T, Ellard, Sian, Shaw-Smith, Charles J
المصدر: European Journal of Human Genetics; Dec2015, Vol. 23 Issue 12, p1744-1748, 5p
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2دورية أكاديمية
المؤلفون: Evers, Christina, Paramasivam, Nagarajan, Hinderhofer, Katrin, Fischer, Christine, Granzow, Martin, Schmidt-Bacher, Annette, Eils, Roland, Steinbeisser, Herbert, Schlesner, Matthias, Moog, Ute
المصدر: European Journal of Human Genetics; Dec2015, Vol. 23 Issue 12, p1627-1633, 7p
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3دورية أكاديمية
المؤلفون: Bosch, Daniëlle G M, Boonstra, F Nienke, Kinoshita, Taroh, Jhangiani, Shalini, de Ligt, Joep, Cremers, Frans P M, Lupski, James R, Murakami, Yoshiko, de Vries, Bert B A
المصدر: European Journal of Human Genetics; Dec2015, Vol. 23 Issue 12, p1689-1693, 5p
مصطلحات موضوعية: GENETIC disorders, HUMAN genetic variation, VISION disorders, INTELLECTUAL disabilities, BIOSYNTHESIS, CELL lines
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4دورية أكاديمية
المؤلفون: Ferri, Lorenzo, Donati, Maria A, Funghini, Silvia, Cavicchi, Catia, Pensato, Viviana, Gellera, Cinzia, Natacci, Federica, Spaccini, Luigina, Gasperini, Serena, Vaz, Frédéric M, Cooper, David N, Guerrini, Renzo, Morrone, Amelia
المصدر: European Journal of Human Genetics; Dec2015, Vol. 23 Issue 12, p1708-1712, 5p
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5دورية أكاديمية
المؤلفون: Fennell, Nathalie, Foulds, Nicola, Johnson, Diana S, Wilson, Louise C, Wyatt, Michelle, Robertson, Stephen P, Johnson, David, Wall, Steven A, Wilkie, Andrew OM
المصدر: European Journal of Human Genetics; Dec2015, Vol. 23 Issue 12, p1684-1688, 5p
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6دورية أكاديمية
المؤلفون: Tønne, Elin, Holdhus, Rita, Stansberg, Christine, Stray-Pedersen, Asbjørg, Petersen, Kjell, Brunner, Han G, Gilissen, Christian, Hoischen, Alexander, Prescott, Trine, Steen, Vidar M, Fiskerstrand, Torunn
المصدر: European Journal of Human Genetics; Dec2015, Vol. 23 Issue 12, p1652-1656, 5p
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7دورية أكاديمية
المؤلفون: Pirim, Dilek, Wang, Xingbin, Radwan, Zaheda H, Niemsiri, Vipavee, Bunker, Clareann H, Barmada, M Michael, Kamboh, M Ilyas, Demirci, F Yesim
المصدر: European Journal of Human Genetics; Sep2015, Vol. 23 Issue 9, p1244-1253, 10p
مصطلحات موضوعية: BLOOD lipids, LIPOPROTEINS, CHOLESTEROL, GENETIC testing, GENETIC disorders, GENETIC mutation
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8دورية أكاديمية
المؤلفون: Bullich, Gemma, Trujillano, Daniel, Santín, Sheila, Ossowski, Stephan, Mendizábal, Santiago, Fraga, Gloria, Madrid, Álvaro, Ariceta, Gema, Ballarín, José, Torra, Roser, Estivill, Xavier, Ars, Elisabet
المصدر: European Journal of Human Genetics; Sep2015, Vol. 23 Issue 9, p1192-1199, 8p
مصطلحات موضوعية: NEPHROTIC syndrome, KIDNEY diseases, KIDNEY glomerulus, GENETIC mutation, GENETIC disorders
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9دورية أكاديمية
المؤلفون: Tan-Sindhunata, M Brigita, Mathijssen, Inge B, Smit, Margriet, Baas, Frank, de Vries, Johanna I, van der Voorn, J Patrick, Kluijt, Irma, Hagen, Marleen A, Blom, Eveline W, Sistermans, Erik, Meijers-Heijboer, Hanne, Waisfisz, Quinten, Weiss, Marjan M, Groffen, Alexander J
المصدر: European Journal of Human Genetics; Sep2015, Vol. 23 Issue 9, p1151-1157, 7p
مصطلحات موضوعية: GENETIC testing, GENETIC disorders, GENETIC mutation, PROTEIN-tyrosine kinases, SYNAPTOGENESIS
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10دورية أكاديمية
المؤلفون: Barthélémy, Florian, Navarro, Claire, Fayek, Racha, Da Silva, Nathalie, Roll, Patrice, Sigaudy, Sabine, Oshima, Junko, Bonne, Gisèle, Papadopoulou-Legbelou, Kyriaki, Evangeliou, Athanasios E, Spilioti, Martha, Lemerrer, Martine, Wevers, Ron A, Morava, Eva, Robaglia-Schlupp, Andrée, Lévy, Nicolas, Bartoli, Marc, De Sandre-Giovannoli, Annachiara
المصدر: European Journal of Human Genetics; Aug2015, Vol. 23 Issue 8, p1051-1061, 11p
مصطلحات موضوعية: PROGERIA, PREMATURE aging (Medicine), GENETIC disorders, NUCLEAR deformation, DNA damage