-
1دورية أكاديمية
المصدر: Cells; Volume 11; Issue 12; Pages: 1886
مصطلحات موضوعية: IGF2, growth, Silver–Russell syndrome, Beckwith–Wiedemann syndrome, parental imprinting
وصف الملف: application/pdf
العلاقة: Cellular Aging; https://dx.doi.org/10.3390/cells11121886Test
-
2دورية أكاديمية
المصدر: Cells, Vol 11, Iss 1886, p 1886 (2022)
مصطلحات موضوعية: IGF2, growth, Silver–Russell syndrome, Beckwith–Wiedemann syndrome, parental imprinting, Cytology, QH573-671
العلاقة: https://www.mdpi.com/2073-4409/11/12/1886Test; https://doaj.org/toc/2073-4409Test; https://doaj.org/article/a746b99110ee4c9eb8d95958d314f495Test
الإتاحة: https://doi.org/10.3390/cells11121886Test
https://doaj.org/article/a746b99110ee4c9eb8d95958d314f495Test -
3دورية أكاديمية
المؤلفون: Aurelie Pham, Delphine Mitanchez, Anne Forhan, Laurence Perin, Yves Le Bouc, Frederic Brioude, Marie-Laure Sobrier, Barbara Heude, Irene Netchine
المصدر: Frontiers in Endocrinology, Vol 13 (2022)
مصطلحات موضوعية: DLK1, small for gestational age (SGA), fetal growth restriction, placental vascular dysfunction, biomarker, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
العلاقة: https://www.frontiersin.org/articles/10.3389/fendo.2022.836731/fullTest; https://doaj.org/toc/1664-2392Test; https://doaj.org/article/54434e9b12d244b4afc959af61b29a70Test
الإتاحة: https://doi.org/10.3389/fendo.2022.836731Test
https://doaj.org/article/54434e9b12d244b4afc959af61b29a70Test -
4دورية أكاديمية
المؤلفون: Eloïse Giabicani, Sandra Chantot-Bastaraud, Adeline Bonnard, Myriam Rachid, Sandra Whalen, Irène Netchine, Frédéric Brioude
المصدر: Frontiers in Endocrinology, Vol 10 (2019)
مصطلحات موضوعية: Beckwith-Wiedemann syndrome, IGF1 receptor, IGF-II, fetal growth restriction, imprinting disease, 11p duplication, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
العلاقة: https://www.frontiersin.org/article/10.3389/fendo.2019.00263/fullTest; https://doaj.org/toc/1664-2392Test; https://doaj.org/article/90c82a8e25934b0eacab6d906a29c214Test
الإتاحة: https://doi.org/10.3389/fendo.2019.00263Test
https://doaj.org/article/90c82a8e25934b0eacab6d906a29c214Test -
5دورية أكاديمية
المؤلفون: Sandra Chantot-Bastaraud, Svea Stratmann, Frédéric Brioude, Matthias Begemann, Miriam Elbracht, Luitgard Graul-Neumann, Madeleine Harbison, Irène Netchine, Thomas Eggermann
المصدر: Molecular Cytogenetics, Vol 10, Iss 1, Pp 1-7 (2017)
مصطلحات موضوعية: Maternal uniparental Disomy 7, Formation mechanism, Chromosome 7, Trisomic rescue, Genetics, QH426-470
العلاقة: http://link.springer.com/article/10.1186/s13039-017-0329-1Test; https://doaj.org/toc/1755-8166Test; https://doaj.org/article/84c97e1f32fb43759434f5e53211c1a6Test
الإتاحة: https://doi.org/10.1186/s13039-017-0329-1Test
https://doaj.org/article/84c97e1f32fb43759434f5e53211c1a6Test -
6دورية أكاديمية
المؤلفون: Frédéric Brioude, Jérôme Bouligand, Bruno Francou, Jérôme Fagart, Ronan Roussel, Say Viengchareun, Laurent Combettes, Sylvie Brailly-Tabard, Marc Lombès, Jacques Young, Anne Guiochon-Mantel
المصدر: PLoS ONE, Vol 8, Iss 1, p e53896 (2013)
العلاقة: http://europepmc.org/articles/PMC3548821?pdf=renderTest; https://doaj.org/toc/1932-6203Test; https://doaj.org/article/40b7198a37f6439d9dc1cd1d50c97c53Test
الإتاحة: https://doi.org/10.1371/journal.pone.0053896Test
https://doaj.org/article/40b7198a37f6439d9dc1cd1d50c97c53Test