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: Melita Irving, Sylvie Rossignol, Azzi Salah, Catherine Vincent-Delorme, Olimpia Chivu, Jean-Louis Plennevaux, Owen Miller, Sylvie Manouvrier, Mustafa Ghanim, Bruno Delobel, Irene Netchine, Sophie Lucidarme-Rossi, Louise Devisme

المصدر: American Journal of Medical Genetics Part A. 161:572-577

مصطلحات موضوعية: Heart Defects, Congenital, Male, medicine.medical_specialty, Pediatrics, Disease, Biology, Cor Triatriatum Sinistrum, Total anomalous pulmonary venous return, Fatal Outcome, Growth restriction, Internal medicine, parasitic diseases, Genotype, Genetics, medicine, Humans, Abnormalities, Multiple, Genetic Association Studies, Genetics (clinical), Chromosome 7 (human), Chromosomes, Human, Pair 11, Silver–Russell syndrome, Infant, Newborn, DNA Methylation, medicine.disease, Silver-Russell Syndrome, Endocrinology, Child, Preschool, Cor triatriatum, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63a7c86b31ea4d05b1d8e5026c47e91aTest
https://doi.org/10.1002/ajmg.a.35691Test