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

المؤلفون: Demars, Julie, Shmela, Mansur Ennuri, Khan, Abdul Waheed, Lee, Kai Syin, Azzi, Salah, Dehais, Patrice, Netchine, Irène, Rossignol, Sylvie, Le Bouc, Yves, El Osta, Assam, Gicquel, C.

المساهمون: Génétique Physiologie et Systèmes d'Elevage (GenPhySE ), Institut National de la Recherche Agronomique (INRA)-Ecole Nationale Vétérinaire de Toulouse (ENVT), Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Université de Toulouse (UT)-École nationale supérieure agronomique de Toulouse (ENSAT), Université de Toulouse (UT)-Université de Toulouse (UT), Baker IDI Heart and Diabetes Institute, Monash University, University of Melbourne, Centre de Recherche Saint-Antoine (CRSA), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), National Health and Medical Research Council of Australia 472637, Victorian Government's Operational Infrastructure Support Program, Institut National de la Sante et de la Recherche Medicale UMPC -Paris6, ANR EPIFEGRO, Pfizer, Agence de Biomedecine

المصدر: ISSN: 0022-2593.

مصطلحات موضوعية: fetal growth disorder, tightly linked marker, dna methylation, haplotype, silver russell syndrome, [SDV]Life Sciences [q-bio], [INFO]Computer Science [cs]

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24996904; hal-02640231; https://hal.inrae.fr/hal-02640231Test; PRODINRA: 265694; PUBMED: 24996904; WOS: 000339271200002

الإتاحة: https://doi.org/10.1136/jmedgenet-2014-102368Test
https://hal.inrae.fr/hal-02640231Test

المؤلفون: Demars, Julie, Shmela, Mansur Ennuri, Khan, Abdul Waheed, Lee, Kai Syin, Azzi, Salah, Dehais, Patrice, Netchine, Iréne, Rossignol, Sylvie, Bouc, Yves Le, El-Osta, Assam, Gicquel, Christine

المصدر: Journal of Medical Genetics; Aug2014, Vol. 51 Issue 8, p502-511, 10p

مصطلحات موضوعية: BECKWITH-Wiedemann syndrome, FETAL growth disorders, DNA methylation, HAPLOTYPES, GENOMICS

المؤلفون: Azzi, Salah, Steunou, Virginie, Rousseau, Alexandra, Rossignol, Sylvie, Thibaud, Nathalie, Danton, Fabienne, Le Jule, Marilyne, Gicquel, Christine, Le Bouc, Yves, Netchine, Irène

المصدر: Human Mutation; Feb2011, Vol. 32 Issue 2, p249-258, 10p

المؤلفون: Keren, Boris^1,2,3, Chantot-Bastaraud, Sandra^4,5, Brioude, Frédéric^2,6,7, Mach, Corinne¹, Fonteneau, Eric¹, Azzi, Salah^6,7, Depienne, Christel^1,2,3, Brice, Alexis^1,2,3, Netchine, Irène^2,6,7, Le Bouc, Yves^2,6,7, Siffroi, Jean-Pierre^2,4,5, Rossignol, Sylvie^2,6,7 sylvie.rossignol@trs.aphp.fr

المصدر: European Journal of Medical Genetics. Oct2013, Vol. 56 Issue 10, p546-550. 5p.

مصطلحات موضوعية: *PROTEUS syndrome, *SINGLE nucleotide polymorphisms, *DNA microarrays, *TUMORS in children, *GENE expression, *EPIGENETICS, *DNA methylation, *DIAGNOSIS, *TUMOR risk factors