المؤلفون: Demars, Julie, Rossignol, Sylvie, Netchine, Irène, Syin Lee, Kai, Shmela, Mansur, Faivre, Laurence, Weill, Jacques, Odent, Sylvie, Azzi, Salah, Callier, Patrick, Lucas, Josette, Dubourg, Christèle, Andrieux, Joris, Le Bouc, Yves, El-Osta, Assam, Gicquel, Christine

المساهمون: Epigenetics in Human Health and Disease, Baker IDI Heart and Diabetes Institute, Centre de Recherche Saint-Antoine (UMRS893), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Experimental Cardiology, Academic Medical Center - Academisch Medisch Centrum Amsterdam (AMC), University of Amsterdam Amsterdam = Universiteit van Amsterdam (UvA)-University of Amsterdam Amsterdam = Universiteit van Amsterdam (UvA)-Heart Failure Research Center (HFRC), Service d'endocrinologie pédiatrique CHU Lille, Hôpital Jeanne de Flandre Lille -Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille), Service de génétique clinique Rennes, Université de Rennes (UR)-Centre Hospitalier Universitaire de Rennes CHU Rennes = Rennes University Hospital Ponchaillou -hôpital Sud, Laboratoire de cytogénétique (CHU de Dijon), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Service de Cytogénétique et de Biologie Cellulaire, Université de Rennes (UR)-Centre Hospitalier Universitaire de Rennes CHU Rennes = Rennes University Hospital Ponchaillou, Laboratoire de génétique moléculaire et génomique médicale CHU Rennes, Centre Hospitalier Universitaire de Rennes CHU Rennes = Rennes University Hospital Ponchaillou, Laboratoire de Génétique Clinique, Hôpital Jeanne de Flandre Lille -Université de Lille, Droit et Santé-Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille), This work was supported by the National Health and Medical Research Council of Australia (Project grant 472637), the Baker IDI Heart and Diabetes Institute, the Institut National de la Santé et de la Recherche Médicale UMPC U938, Université Pierre et Marie Curie Paris 6 and Assistance Publique Hopitaux de Paris.

المصدر: ISSN: 1059-7794.

مصطلحات موضوعية: fetal growth, genomic imprinting, copy number variation, 11p15 region, Silver-Russell syndrome, Beckwith-Wiedemann syndrome, MESH: Base Sequence, MESH: Male, MESH: Pedigree, MESH: Polymorphism, Single Nucleotide, MESH: Silver-Russell Syndrome, MESH: Adult, MESH: Beckwith-Wiedemann Syndrome, MESH: Chromosomes, Human, Pair 11, MESH: Comparative Genomic Hybridization, MESH: DNA Copy Number Variations, MESH: DNA Methylation, MESH: Female, MESH: Genomic Imprinting, MESH: Humans, [SDV.GEN]Life Sciences [q-bio]/Genetics, [SDV.BDD]Life Sciences [q-bio]/Development Biology

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21780245; inserm-00610827; https://inserm.hal.science/inserm-00610827Test; https://inserm.hal.science/inserm-00610827/documentTest; https://inserm.hal.science/inserm-00610827/file/CNV_manuscript_14122010.pdfTest; PUBMED: 21780245

الإتاحة: https://doi.org/10.1002/humu.21558Test
https://inserm.hal.science/inserm-00610827Test
https://inserm.hal.science/inserm-00610827/documentTest
https://inserm.hal.science/inserm-00610827/file/CNV_manuscript_14122010.pdfTest

المؤلفون: Abi Habib, Walid, Brioude, Frédéric, Azzi, Salah, Rossignol, Sylvie, Linglart, Agnès, Sobrier, Marie-Laure, Giabicani, Éloïse, Steunou, Virginie, Harbison, Madeleine D., Le Bouc, Yves, Netchine, Irène

المساهمون: Centre de Recherche Saint-Antoine (CR Saint-Antoine), Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Saint-Antoine [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Les Hôpitaux Universitaires de Strasbourg (HUS), AP-HP Hôpital Bicêtre (Le Kremlin-Bicêtre), Icahn School of Medicine at Mount Sinai [New York] (MSSM)

المصدر: Science Advances
Science Advances, American Association for the Advancement of Science (AAAS), 2019, 5 (2), pp.eaau9425. ⟨10.1126/sciadv.aau9425⟩

مصطلحات موضوعية: Chromosomes, Human, Pair 14, Male, Chromosomes, Human, Pair 11, Calcium-Binding Proteins, SciAdv r-articles, Membrane Proteins, Human Genetics, DNA Methylation, Epigenesis, Genetic, Genomic Imprinting, Silver-Russell Syndrome, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], parasitic diseases, Humans, Female, Research Articles, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::90203985169791de2c169a06531f9006Test
https://hal.sorbonne-universite.fr/hal-02090873/documentTest

المؤلفون: Maupetit‐Méhouas, Stéphanie, Azzi, Salah, Steunou, Virginie, Sakakini, Nathalie, Silve, Caroline, Reynes, Christelle, Perez de Nanclares, Guiomar, Keren, Boris, Chantot, Sandra, Barlier, Anne, Linglart, Agnès, Netchine, Irène

المصدر: Human Mutation; Aug2013, Vol. 34 Issue 8, p1172-1180, 9p