Netchine,Irene

Institution: APHP, Hôpital Armand Trousseau, Laboratoire d'Explorations Fonctionnelles Endocriniennes, INSERM UMR-S938 Team 4, Université Pierre et Marie Curie-Paris 6, Paris, France

Research Interests: Silver, Patients, Methylation, Syndrome, Beckwith Wiedemann Syndrome, Genomic Imprinting, Human, Syndromes, Cancers, Diseases, Phenotype, Risk, Epigenetic, Identification, Lead, Regulation, Russell Silver Syndrome, Understanding, Allele, Beckwith-wiedemann Syndrome