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pro vyhledávání: '"Bizaoui, Varoona"'
Autor:
Bizaoui V; Department of Medical Genetics, Reference Center for Skeletal Dysplasia and OSCAR Network, Paris Descartes-Sorbonne Paris Cité University, INSERM UMR 1163, Instititut Imagine, Hôpital Necker Enfants Malades, Paris, France., Michot C; Department of Medical Genetics, Reference Center for Skeletal Dysplasia and OSCAR Network, Paris Descartes-Sorbonne Paris Cité University, INSERM UMR 1163, Instititut Imagine, Hôpital Necker Enfants Malades, Paris, France., Baujat G; Department of Medical Genetics, Reference Center for Skeletal Dysplasia and OSCAR Network, Paris Descartes-Sorbonne Paris Cité University, INSERM UMR 1163, Instititut Imagine, Hôpital Necker Enfants Malades, Paris, France., Amouroux C; Department of Paediatric Endocrinology, Arnaud de Villeneuve Hospital, Montpellier, France., Baron S; Service de Génétique Médicale, CHU de Nantes, Nantes, France., Capri Y; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France., Cohen-Solal M; Department of Rheumatology, Lariboisière Hospital, INSERM U1132 and University Paris-Diderot, Paris, France., Collet C; Department of Biochemistry, APHP, Saint-Louis Lariboisière Hospitals, Paris, France., Dieux A; Centre de Référence CLAD NdF, Service de Génétique Clinique, Hôpital Jeanne de Flandre, CHU Lille, France., Geneviève D; Service de Génétique Clinique et du Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Centre de Compétence Maladies Osseuses Constitutionnelles, Inserm U1183, Université Montpellier, Montpellier, France., Isidor B; Service de Génétique Médicale, CHU de Nantes, Nantes, France., Monnot S; Department of Medical Genetics, Reference Center for Skeletal Dysplasia and OSCAR Network, Paris Descartes-Sorbonne Paris Cité University, INSERM UMR 1163, Instititut Imagine, Hôpital Necker Enfants Malades, Paris, France., Rossi M; Hospices Civils de Lyon, Service de Génétique, Centre de Référence Anomalies du Développement, Bron, France.; Centre de Recherche en Neurosciences de Lyon, INSERM U1028, CNRS UMR5292, UCB Lyon 1, Lyon, France., Rothenbuhler A; Department of Paediatric Endocrinology, Bicêtre Hospital, Paris, France., Schaefer E; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France., Cormier-Daire V; Department of Medical Genetics, Reference Center for Skeletal Dysplasia and OSCAR Network, Paris Descartes-Sorbonne Paris Cité University, INSERM UMR 1163, Instititut Imagine, Hôpital Necker Enfants Malades, Paris, France.
Publikováno v:
Clinical genetics [Clin Genet] 2019 Oct; Vol. 96 (4), pp. 309-316. Date of Electronic Publication: 2019 Jun 25.