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1دورية أكاديمية
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 -
2دورية أكاديمية
المؤلفون: Netchine, Irène, Azzi, Salah, Le Bouc, Yves, Savage, Martin O.
المصدر: Best Practice & Research Clinical Endocrinology & Metabolism; Feb2011, Vol. 25 Issue 1, p181-190, 10p
مصطلحات موضوعية: SOMATOTROPIN, HUMAN genetics, NEURAL development, GESTATIONAL age, FETAL growth retardation, SHORT stature, MICROCEPHALY, DEAFNESS